The biology of neurotypical (allistic) brains is towards maximal efficiency. Microglia literally prune redundant synapses to strengthen neural connections. This works differently in autistic folks who have many more dendritic spines & less pruning🧵
Paper: nature.com/articles/nn.27…
2/ These brains function differently. Many folks have superior pattern recognition. It’s not fully understood why. Some areas of the brain have shown more connectivity, some less. Many variables at play and lack of diagnosis especially in underrepresented groups are significant.
3/ Some literature cites higher incidence of neurodegenerative diseases in Autistic people but with the known diagnostic and representation issues, as well as how much we don’t understand about the brain, I’m not sure how much of that can be extrapolated to an entire population.
4/ Got me thinking, as most things do…nature holds onto things that have an evolutionary advantage. Humans used to live to be only 30 or 40 years old. But now we have doubled that life span. In doing so, we face neurodegeneration and diseases that accelerate that neural pruning.
5/ Traits that have an evolutionary advantage or benefit are conserved.
For example, similar to our own circulatory system, leaf veins and capillaries have multiple connections and alternative pathways/loops in case part of the leaf gets damaged.
6/ This is a different pattern than the branching of tree limbs or root systems.
What if the brain hyper connectivity or redundancy in neurodiverse individuals is actually protective against neurodegeneration and brain injury?
What if infectious disease can alter this biology?
7/ Limiting sensory input: routines, foods, environments could allow for greater daily functioning in context of this baseline hyper-connectivity.
Hypersensitivity could be beneficial to survival and to protect human groups during less sensory/stimulating times like at night.
8/ Hyperfocused pattern seekers also notice when things are even slightly off and could function as an early alert system, which could again be protective.
Again, these traits have been evolutionarily conserved - so not accidental and likely beneficial somehow.
This is a really interesting thread on eugenics but has some glaring omissions like the connection with the current pandemic, ongoing US taxpayer funded genocide of Palestine, or that our country was founded on the genocide of Indigenous Americans and built by enslaved Africans🧵
2/ The glaring foundation of white supremacy, colonialism, patriarchy, ableism and capitalism should also be emphasized. Nazi propaganda of “useless eaters” is particularly relevant to our current moment in justifying the mass death of disabled people (as we disable more people)
3/ One could practically do a dissertation on the pandemic specifically explaining the harmful rhetoric and messaging from our administration, Walensky & Fauci regarding eugenics of “the vulnerable” when it’s *society* that MAKES people vulnerable
It has *ALWAYS* been a workers rights issue. One could argue one of the largest in history.
If the people in power won’t protect themselves or their own families from infection, how little do you think they care about you and me? They prioritized “the economy” above all else.
Computer based tests like this exist and patients can do them remotely at home. Because many patients with LC are severely disabled and just getting to a clinic is cognitively and physically exhausting.
The discovery of Hep B Virus was an EMBARASSMENT to @theNCI exactly because of the heavily funded and largely failed *Special Virus Cancer Program* from a scientist who LEFT the NCI in the 1960s exactly because of his interdisciplinary curiosity! Work that led to the HBV vaccine.
@theNCI The first virus discovered to cause cancer in humans was EBV (virus that causes mono) and Burkitt’s Lymphoma in 1958 by an Irish surgeon, Dennis Burkitt and two British virologists.
Caused a whole scurry of chaos with media printing “Cancer may be infectious!” in @LIFEmagazine.
“According to our results, the brains of dogs infected with SARS-CoV-2 demonstrate severe BBB disruptions and consequent SVD-like pathologic signs, including axonopathy, glial activation, and potential neurodegenerative changes even WITHOUT neurologic signs.” #Asymptommatic #MILD
It’s been over 3 years since my review of the initial SARSCOV2 neuro case studies came out.
But now we’ve got autopsy studies and non-human primate studies showing virus in the brain (h/t @DaniBeckman)
And a dog model showing asymptomatic infection resulting in brain damage.
2/ The authors pose the question regarding potential neuropathological mechanisms other than neuronal cell death that help viruses spread infection within the host that then leads to brain dysfunction
Instead of multiplying inside the cell and requiring the cell to burst & die in order to spread virions, the virus actually keeps the cell alive & uses it like a little trojan horse that docks on other similar neurons & fuses with them to