COVID Update: The studies emerging now simply show likely devastating adverse effect(s) for many of the "vaxxed." Given the different batches, it's a bit like Russian Roulette.
ALL of it bad news long-term. The scope of the lies told about C-19 Vaccine "safety" and the gullibility of those who have taken the Vaxx is beyond comprehension. Thanks to Gabi for her sourcing...
How long COVID could change the way we think about disability
Mallory Stanislawczyk was hesitant to make the call. She hadn't spoken to her friend for years. But the friend, who gets around in a wheelchair, was the only person the 34-year-old nurse practitioner could think of who would understand her questions. About being ready to accept help. About using a wheelchair. And about the new identity her battle with long COVID had thrust on her.
"I think she is the first person I said to, 'I'm disabled now’," Stanislawczyk recalled telling the friend. "'And I'm working on accepting that."
The coronavirus pandemic has created a mass-disabling event that experts liken to HIV, polio, or World War II, with millions suffering the long-term effects of infection with the coronavirus. Many have found their lives dramatically changed and are grappling with what it means to be disabled.
"It's an entirely new identity," Stanislawczyk said.
The dramatic influx of newly disabled Americans changes the calculus for disability advocates, who have in recent years been uniting around a shared identity, pushing back against historic marginalization by affirming their self-worth and embracing their disabilities.
Please click on the image for a link to the article…
Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19
Stephanie Seneff Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge MA, 02139, USA
Greg Nigh Naturopathic Oncology, Immersion Health, Portland, OR 97214, USA
Abstract
Operation Warp Speed brought to market in the United States two (2) mRNA vaccines, produced by Pfizer and Moderna.
Interim data suggested high efficacy for both of these vaccines, which helped legitimize the Emergency Use Authorization (EUA) by the FDA. However, the exceptionally rapid movement of these vaccines through controlled trials and into mass deployment raises multiple safety concerns.
In this review, we first describe the technology underlying these vaccines in detail. We then review both components of and the intended biological response to these vaccines, including the production of the spike protein itself, and their potential relationship to a wide range of both acute and long-term induced pathologies, such as blood disorders, neurodegenerative diseases, and autoimmune diseases. Among these potential induced pathologies, we discuss the relevance of prion-protein-related amino acid sequences within the spike protein.
We also present a brief review of studies supporting the potential for spike protein “shedding”, the transmission of the protein from a vaccinated to an unvaccinated person, resulting in symptoms induced in the latter.
We finish by addressing a common point of debate, namely, whether or not these vaccines could modify the DNA of those receiving the vaccination. While there are no studies demonstrating definitively that this is happening, we provide a plausible scenario, supported by previously established pathways for transformation and transport of genetic material, whereby injected mRNA could ultimately be incorporated into germ cell DNA for transgenerational transmission.
We conclude with our recommendations regarding surveillance that will help to clarify the long-term effects of these experimental drugs and allow us to better assess the true risk/benefit ratio of these novel technologies.
Please click on the image for a link to the article…
Facts about variant Creutzfeldt-Jakob disease
Variant Creutzfeldt-Jakob disease (vCJD) is a relatively new and rare neurological disease, classified as a Transmissible Spongiform Encephalopathy (TSE). It was first identified in March 1996 in the UK, when 10 cases of a new disease with neurological symptoms were reported and soon associated with the Bovine Spongiform Encephalopathy (BSE), “mad cow”-disease.
Causative agents of vCJD are prions, composed of misfolded prion proteins (PrPSc), which form aggregates in neurological tissue leading to progressive brain damage and characteristic signs and symptoms of the disease. Prions are stable and relatively resistant to proteases, high temperatures, UV radiation, and commonly used disinfectants.
Patients with vCJD have prominent psychiatric (frequently depression, anxiety, and withdrawal) or sensory symptoms and delayed onset of neurologic abnormalities, including ataxia within weeks or months, and dementia and myoclonus late in the illness. The disease always progresses to death. Disease duration is 14 months on average. vCJD tends to affect younger individuals, with an average age of onset of around 28 years, compared to sporadic CJD, which tends to affect middle-aged and elderly individuals.
The definite diagnosis of vCJD requires a post-mortem examination of brain tissue.
The incubation period for vCJD after food-borne exposure is thought to be around 10 years. No vaccine or treatment is available.
Most reported vCJD cases appear to have been infected through the consumption of bovine meat products contaminated with the agent of BSE. In three cases, reported by the UK, the mode of transmission is thought to be through receipt of blood from an asymptomatic, infected donor.
Please click on the image for a link to the article…
COVID Vaccines Linked to New Type of Incurable, Fatal Degenerative Brain Disorder
And the hits keep comin’…~TS
Studies suggest a link between a rapidly progressing, incurable, and fatal prion disease known as Creutzfeldt-Jakob Disease and COVID-19 vaccines.
By Megan Redshaw | The Defender
Studies suggest a link between an incurable and fatal prion disease known as Creutzfeldt-Jakob Disease (CJD) and COVID-19 vaccines.
Researchers believe the prion region from the original Wuhan COVID-19 variant’s spike protein was incorporated into mRNA vaccines and adenovirus vector vaccines — given to hundreds of millions of humans — and that it can cause a new type of rapidly progressing sporadic CJD.
According to Mayo Clinic, CJD is a degenerative brain disorder that leads to dementia and, ultimately, death.
Although the Omicron variant does not have a prion region on its spike protein, current COVID-19 vaccines still use the genetic material — including the prion region — of the parent Wuhan strain.
A French pre-print paper published in May on CJD and COVID-19 vaccination identified a new form of sporadic CJD that occurred within days of receiving a first or second dose of Pfizer or Moderna COVID-19 vaccines.
Researchers analyzed 26 cases of CJD and found the first symptoms appeared on average 11.38 days after injection with a COVID-19 vaccine.
Of the 26 cases, 20 had died by the time the study was published and six were still alive.
“The 20 deaths occurred only 4.76 months after the injection. Among them, 8 of them lead to sudden death (2.5 months),” researchers wrote.
“This confirms the radically different nature of this new form of CJD, whereas the classic form requires several decades,” wrote the researchers.
Dr. Jean-Claude Perez, lead author of the French study, on June 6 told The Epoch Times that all 26 cases resulted in death.
According to the Centers for Disease Control and Prevention (CDC), prion diseases are a family of rare progressive neurodegenerative disorders that affect humans and animals. Prion diseases are usually rapidly progressive and always fatal.
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Prion-like Domains in Spike Protein of SARS-CoV-2 Differ across Its Variants and Enable Changes in Affinity to ACE2
Abstract
Currently, the world is struggling with the coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Prions are proteins that possess a unique conformational conversion, with the ability to rapidly shift between multiple conformations due to residue hydrophobicity and net sequence charge, and viral prion-like proteins are known as potential regulators of viral infections. However, the prion-like domains (PrD) in the SARS-CoV-2 proteome have not been analyzed.
In this in silico study, using the PLAAC algorithm, we identified the presence of prion-like domains in the SARS-CoV-2 spike protein. Compared with other viruses, a striking difference was observed in the distribution of prion-like domains in the spike protein since SARS-CoV-2 is the only coronavirus with a prion-like domain found in the receptor-binding domain of the S1 region of the spike protein.
The presence and unique distribution of prion-like domains in the SARS-CoV-2 receptor-binding domains of the spike protein are particularly interesting since although the SARS-CoV-2 and SARS-CoV S proteins share the same host cell receptor, angiotensin-converting enzyme 2 (ACE2), SARS-CoV-2 demonstrates a 10- to 20-fold higher affinity for ACE2.
We identified prion-like domains in the α1 helix of the ACE2 receptor that interact with the viral receptor-binding domain of SARS-CoV-2.
Finally, we found substantial differences in the prion-like domain of the S1 region of the spike protein across emerging variants including Omicron (B.1.1.529).
Taken together, the present findings indicate that the identified PrDs in the SARS-CoV-2 receptor-binding domain (RBD) and ACE2 region that interact with RBD play important functional roles in viral adhesion and entry.
Please click on the image for a link to the article…
The Medicare Data: How Can You Explain a 50% Rise in All-Cause Mortality for an Intervention?
Steve Kirsch: (http://t.me/stkirsch)
"How can you explain a 50% rise in all-cause mortality after the vaccines and boosters rolled out?
That's the problem. They can't explain it.
You can't explain a 50% rise in all-cause mortality after the intervention that's supposed to reduce all-cause mortality was rolled out. They don't want to explain it. That is why they are never going to show you the Medicare data."
Please click on the image for a link to this very short yet impactful video… (01:25)