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From the paper “The Neurobiology of Long COVID”:

Demonstrated effects of reactive microglia after COVID-19 include a reduction in oligodendrocytes and myelinated axons, highlighting disrupted myelin homeostasis.

The UK Biobank study discussed above compared magnetic resonance imaging (MRI) data before and after SARS-CoV-2 infection in 401 individuals and 385 matched controls. MRI data obtained an average of 141 days following COVID-19 diagnosis revealed widespread structural abnormalities, including a small but significant global decrease in brain volume, changes throughout the olfactory system, and structural abnormalities in the limbic system, cerebellum, and major white matter tracts (fimbria and superior fronto-occipital fasciculus)

Concordant findings in an MRI study of individuals with persistent cognitive impairment after COVID-19 found white matter hyperintensities correlating with verbal memory deficits

Another imaging and neuropsychological assessment of 223 individuals who recovered from mainly mild to moderate SARS-CoV-2 infections and 223 matched healthy controls found that among the 11 MRI markers tested, significant differences between groups were found in global measures of mean diffusivity and extracellular free water, which were both elevated in the white matter of post-SARS-CoV-2 individuals

And so on and so forth. Those are the first immediately obvious passages describing structural alterations to brain tissue in that one paper.

These are severe physiological issues. This is literal brain damage. This is a paper pointing to craters.



Will CBT help with impaired oxygen perfusion of tissue caused by a pathogen known to cause pervasive vascular damage and severely deranged blood clotting?

https://www.sciencedirect.com/science/article/pii/S002628622...


Also, why does CBT work when it does?

Oxytocin is directly anti-inflammatory and CBT can and does affect oxytocin secretion.

https://www.tandfonline.com/doi/full/10.1080/15374416.2023.2...




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