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.

Wednesday, September 16, 2026

Genetic discovery offers clues for repairing damaged neural connections

I suppose your incompetent? doctor hasn't already provided the needed axon pathfinding protocols! 

AND YOU HAVEN'T FIRED THEM YET?

 Genetic discovery offers clues for repairing damaged neural connections

A new discovery by neuroscientists at Brown University's Carney Institute for Brain Science challenges long-held beliefs in neurobiology about how neurons extend axons to reach their targets.

Published in PNAS, the findings provide what the authors call a "genetic atlas" of neuronal development as well as a potential step forward for understanding how to repair broken neural connections in conditions such as stroke and spinal cord injury.

We discovered that during development, neurons turn on and off entire groups of genes that allow their axons to grow through different sections of their path. That's surprising." 

Alexander Jaworski, study author, associate professor of brain science, Carney Institute

Axons are critical components of neural wiring. During embryonic development, they shoot out from neurons like plant tendrils searching for light, traveling along intricate and sometimes long pathways to reach target cells. For example, the axon of a motor neuron that enables foot movement extends all the way to the foot from the base of the spine.

How are axons capable of making these connections with such precision? Until now, the conventional thinking was that because axons are so long and respond so rapidly to their environment, the guidance about where to grow next must come from the axon tip. 

A team of researchers in Jaworski's lab discovered a new twist: Axons are actually controlled by a genetic switch in the cell body of the neuron.

Prior to this study, researchers knew that part of the secret to an axon's long-distance travel is that they stop at intermediate waystations en route to their destination. As they pass through a waystation, axons pivot as needed to aim for the next one - a process called axon pathfinding.

To understand this process in more depth, the researchers focused on commissural neurons, which connect the left and right sides of the central nervous system. This specific neuron type is particularly useful to study because its axon makes a distinct, sharp change in direction as it crosses the spinal cord midline.

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