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, January 26, 2011

deep brain neurons and stroke rehab research

Visualizing neurons in the deep brain. This technology
sounds like a fascinating way for stroke researchers to
watch neuroplasticity take hold. Between deep brain neurons, connectomics,
and array tomography, one of these should be required for
researchers to prove that therapies work.
Stanford scientists have devised a new method that not only
lets them peer deep inside the brain to examine its neurons
but also allows them to continue monitoring for months.
Because light microscopy can only penetrate the outermost
layer of tissues, any region of the brain deeper than 700
microns or so (about 1/32 of an inch) cannot be reached by
traditional microscopy techniques. Recent advances in micro
-optics had allowed scientists to briefly peer deeper into
living tissues, but it was nearly impossible to return to
the same location of the brain and it was very likely that
the tissue of interest would become damaged or infected.
With the new method, "Imaging is possible over a very long
time without damaging the region of interest," said Juergen
Jung, operations manager of the Schnitzer lab. Tiny glass
tubes, about half the width of a grain of rice, are
carefully placed in the deep brain of an anaesthetized
mouse. Once the tubes are in place, the brain is not exposed
to the outside environment, thus preventing infection. When
researchers want to examine the cells and their interactions
at this site, they insert a tiny optical instrument called a
microendoscope inside the glass guide tube. The guide tubes
have glass windows at the ends through which scientists can
examine the interior of the brain.
"It's a bit like looking through a porthole in a submarine,"
said Schnitzer.

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