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Anonymous ID: 521745 May 6, 2025, 9 a.m. No.22999185   🗄️.is 🔗kun

Top USvirologist Ralph Baric engineered the Covid-19 virus SARS-CoV-2 in his lab at the University of North Carolinaas part of his work in connection with the 2018 DEFUSE funding proposal. That’s the story that’s been going round the internet for some months now (and not just in alternative media) and it all looks very damning for Baric and those connected with his research.

 

Details of the DEFUSE project were first leaked by Major Joseph Murphy, an employee of US military research agency DARPA, in the summer of 2021 and further details of earlier drafts have come to light this month thanks to public record requests from U.S. Right to Know (USRTK).

 

In DEFUSE, Baric proposed to create a virus that was, to most intents and purposes, SARS-CoV-2. The proposal included inserting a furin cleavage site into a coronavirus spike protein, an order for the restrictive enzyme BsmBI, the search for a binding domain that would infect ACE2 human receptors and a requirement for a viral genome around 25% different to SARS.

 

5:27 PM · May 3, 2025·661 Views

https://x.com/dotconnectinga/status/1918779518749491409

Anonymous ID: 521745 May 6, 2025, 9:08 a.m. No.22999213   🗄️.is 🔗kun   >>9215 >>9226 >>9260 >>9293 >>9330 >>9444 >>9515 >>9612 >>9744 >>9815

Nicolas Hulscher, MPH

COVID-19 "Vaccines" Cause Brain Damage.

 

Roh et al found that among 558,017 Koreans, mRNA-injected individuals faced:

 

📈137.7% increased risk of cognitive impairment

 

📈22.5% increased risk of Alzheimer’s disease

 

COVID-19 ‘vaccines’ damage the brain and DEVASTATE mental health. They increase your risk of:

  1. Alzheimer’s (+22.5%),

  2. Cognitive impairment (+137.7%)

  3. Depression (+68.3%)

  4. Anxiety disorders (+43.9%)

  5. Sleep disorders (+93.4%)

This is likely due to toxic Spike protein accumulation and persistence in the skull-meninges-brain axis.

 

5:15 PM · May 2, 2025·77.1K Views

https://x.com/NicHulscher/status/1918414081880670356

Anonymous ID: 521745 May 6, 2025, 9:20 a.m. No.22999260   🗄️.is 🔗kun   >>9293 >>9302 >>9330 >>9338 >>9444 >>9515 >>9612 >>9744 >>9815

>>22999215

>>22999213

Persistence of spike protein at the skull-meningesbrain axis may contribute to the neurological sequelae of COVID-19

 

Highlights

• SARS-CoV-2 spike protein persists in the skull-meninges-brain axis in COVID-19 patients

• Spike protein is sufficient to induce brain pathological and behavioral changes in mice

• Spike protein enhances brain vulnerability and exacerbates neurological damage in mice

• mRNA vaccines reduce, but do not eliminate, the spike burden

 

Summary

SARS-CoV-2 infection is associated with long-lasting neurological symptoms, although the underlying mechanisms remain unclear. Using optical clearing and imaging, we observed the accumulation of SARS-CoV-2 spike protein in the skull-meninges-brain axis of human COVID-19 patients, persisting long after viral clearance. Further, biomarkers of neurodegeneration were elevated in the cerebrospinal fluid from long COVID patients, and proteomic analysis of human skull, meninges, and brain samples revealed dysregulated inflammatory pathways and neurodegeneration-associated changes. Similar distribution patterns of the spike protein were observed in SARS-CoV-2-infected mice. Injection of spike protein alone was sufficient to induce neuroinflammation, proteome changes in the skull-meninges-brain axis, anxiety-like behavior, and exacerbated outcomes in mouse models of stroke and traumatic brain injury. Vaccination reduced but did not eliminate spike protein accumulation after infection in mice. Our findings suggest persistent spike protein at the brain borders may contribute to lasting neurological sequelae of COVID-19.

 

https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(24)00438-4