Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Tuesday, August 12, 2025

The first 25 years of the Northwestern University SuperAging Program

 How EXACTLY is your competent? doctor getting you to be a super ager? NO plans? Then fire that incompetent doctor! I'm going to get there and nothing from my stroke medical 'professionals' has anything to do with that goal.

The first 25 years of the Northwestern University SuperAging Program


Abstract

During late life, “average” does not mean “intact.” For example, cross-sectional data from a common word list learning test show that average delayed word recall raw score at age 80 (5/15) is approximately half that at age 56 to 66 (9/15). Cognitive and neurobiological dissolution is therefore implicitly incorporated into concepts of the aging brain. This position is being challenged through investigations on “superaging,” a term that was coined at the Northwestern Alzheimer's Disease Research Center (ADRC) to define persons ≥ 80 years with delayed word recall raw scores at least equal to those of individuals 20 to 30 years younger. During the first 25 years of this program we established that superagers constitute not only a neuropsychological but also a neurobiological phenotype distinctive from cognitively average age peers. With respect to brain structure, superagers have cortical volumes no different than neurotypical adults 20 to 30 years younger in contrast to neurotypical peers who do show such age-related shrinkage; they also have a region in the cingulate gyrus that is thicker than younger neurotypical adults. With respect to cellular biology, superagers have fewer Alzheimer's disease–type changes in the brain, greater size of entorhinal neurons, fewer inflammatory microglia in white matter, better preserved cholinergic innervation, and a greater density of evolutionarily progressive von Economo neurons. In the future, deeper characterization of the superaging phenotype may lead to interventions that enhance resistance and resilience to involutional changes considered part of average (i.e., “normal”) brain aging. This line of work is helping to revise common misperceptions about the cognitive potential of senescence and has inspired investigations throughout the United States and abroad.

Highlights

  • “Normal cognitive aging” is a term that spans a broad spectrum from average for age to well beyond.
  • “Superaging” at the Northwestern University Alzheimer's Disease Research Center (ADRC) refers to a unique cognitive and biological phenotype.
  • Post mortem findings support resilience and resistance to neuropathologic changes of aging.
More at link.

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