China seriously screwed the world over. I was looking up information on Covid and the vaccine causing chronic inflammation and/or autoimmune responses in folks who had either the vaccine or the virus or both. It seems I have chronic inflammatory response syndrome which can be caused by several things but predominantly mold exposure and Lyme disease but evidence is coming out that Covid and the vaccine can trigger it as well thanks to spike proteins in both. I never got the vaccine but have had the virus twice.
Anyway, I was reading this paper on the National Library of Medicine site that shows just how badly the spike proteins in the virus and the vaccine can affect everyone regardless of age or health status. The following are just the Key Points and they're not encouraging. The ones I bolded are particularly concerning.
The
link to the findings if you have time or care to read it all. Like I said, China screwed humanity hard with this one.
Key Points
Highly safe and effective vaccines are central to combat infectious disease epidemics/pandemics.
SARS-CoV-2 spike protein is pathogenic, whether from the virus or created from genetic code in mRNA and adenovectorDNA vaccines.
Biodistribution rodent study data show lipid nanoparticles carry mRNA to all organs and cross blood-brain and blood-placenta barriers. Some of these tissues are likely to be impervious to viral infection; therefore, the biohazard is particularly from vaccination.
Lipid-nanoparticles have inflammatory properties.
The modification of mRNA with N1-methylpseudouridine for increased stability leads to the production of spike proteins for months. It is uncertain how many cells and from which organs mRNA spike proteins are produced, and therefore, the exact effective dose delivered per vaccine vial is unknown.
The long-term fate of mRNA within cells is currently unknown.
The mRNA and adenovectorDNA vaccines act as ‘synthetic viruses’.
In the young and healthy, and even in many older individuals with vulnerable comorbidities, the encoding-based COVID-19 vaccines will likely transfect a far more diverse set of tissues than infection by the virus itself.
Evidence suggests reverse transcription of mRNA into a DNA copy is possible. This further suggests
the possibility of intergenerational transmission if germline cells incorporate the DNA copy into the host genome.
Production of foreign proteins such as spike protein on cell surfaces can induce autoimmune responses and tissue damage. This has profoundly negative implications for any future mRNA-based drug or vaccine.
The spike protein exerts its pathophysiological effects (‘spikeopathy’) via several mechanisms that lead to inflammation, thrombogenesis, and endotheliitis-related tissue damage and prion-related dysregulation.
Interaction of the vaccine-encoded spike protein with ACE-2, P53 and BRCA1 suggests a wide range of possible biological interference with oncological potential.
Adverse event data from official pharmacovigilance databases, an FDA-Pfizer report obtained via FOI, show high rates and multiple organ systems affected: primarily neurological, cardiovascular, and reproductive.
Pfizer and Moderna mRNA COVID-19 vaccines’ clinical trial data independently interpreted has been peer-review and published to show an unfavourable risk/benefit, especially in the non-elderly. The risks for children clearly outweigh the benefits.
Repeated COVID-19 vaccine booster doses appear to induce tolerance and may contribute to recurrent COVID-19 infection and ‘long COVID’.
The SARS-CoV-2 pandemic has revealed deficiencies in public health and medicines regulatory agencies.
A root cause analysis is needed for what now appears a rushed response to an alarming infectious disease pandemic.
Treatment modalities for ‘spikeopathy’-related pathology in many organ systems, require urgent research and provision to millions of sufferers of long-term COVID-19 vaccine injuries.