Why should we still be interested in the Covid issue, for hasn’t things moved on, and there is nothing more to worry about? If one has been vaxxed and are still not suffering from any adverse effects, why care?
Well, leading Covid medical critic Dr Peter McCullough has a different point of view. He would dispute the claim that the Covid dangers are over. The mRNA spike protein is pathologic, and it is unknown for how long it remains in the body, if it leaves it at all. The spike proteins have been found to migrate to all organs and cross blood-brain and blood-placenta barriers. There is evidence that reverse transcription of mRNA into a DNA copy is possible. If germline cells incorporate the DNA copy into the host genome, there may be intergenerational transmission, affecting the next generation. That is, future children. That should be important.
As said, the long-term effects of the mRNA spike proteins within the human body is not known; this was an experiment conducted upon the entire human race, and we are still in the short-term.
https://petermcculloughmd.substack.com/p/spikeopathy-covid-19-spike-protein
“People commonly ask me for “comprehensive” publications on vaccine side effects. It is fair to point out that the SARS-CoV-2 Spike protein is contained in the virus and it is uncontrollably produced by the mRNA and adenoviral DNA COVID-19 vaccines. Because the vaccines failed to stop COVID-19, most vaccinated persons have had the illness, thereby having multiple Spike protein exposures.
Parry, et al, published a comprehensive review on the litany of Spike-protein diseases that occur after its widespread distribution in the body. Here are some of their evidence based teaching points:
- SARS-CoV-2 spike protein is pathogenic, whether from the virus or created from genetic code in mRNA and adenovector DNA 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 adenovector DNA 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. We also advocate for the suspension of gene-based COVID-19 vaccines and lipid-nanoparticle carrier matrices, and other vaccines based on mRNA or viral-vector DNA technology. A safer course is to use vaccines with well-tested recombinant protein, attenuated or inactivated virus technologies, of which there are now many for vaccinating against SARS-CoV-2.”