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.

Monday, March 26, 2012

New Stroke Recovery Option

Now if someone would have a sense of urgency and get testing in humans.
http://www.ivanhoe.com/channels/p_channelstory.cfm?storyid=29175

There is only one stroke treatment option available today and with such a high rate of individuals suffering from strokes, many would agree that a new solution is necessary.
Now researchers from Stanford University have shown that by removing a matching set of molecules responsible for assisting in regulation of the brain's capacity for forming and breaking connections between nerve cells could greatly increase recovery from a stroke just days after occurring.
Currently the only available stroke treatment is called tissue plasminogen activator, or tPA. The issue with tPA is that it must be administered within a few hours of a stroke to be effective, and patients' brains must first be scanned to determine whether this treatment is appropriate. Furthermore, while tPA limits the initial damage caused by a stroke, it doesn't help the brain restore or replace lost connections between nerve cells, which is necessary for recovery.
For the study, researchers used mice that had been genetically bioengineered to lack certain molecules that a Stanford researcher had previously shown to play a major role in modulating the ease with which important nerve-cell connections are made, strengthened, weakened or destroyed in the brain. The molecules in question include "K" and "D," two of the 50 or so members of the so-called MHC class-1 complex, which plays a key role in the function of the immune system. Alternatively, when a receptor called PirB, which binds to these MHC molecules, is not present, the same improved outcome from stroke happens — significant, because receptors make good drug targets.
Carla Shatz, PhD, professor of neurobiology and of biology, and her colleagues surprised the neuroscience and immunology communities a few years back by showing that these molecules "moonlight" in the brain. Here, their job appears to involve inhibiting the readiness of connections among nerve cells (known as synapses) to grow stronger or weaker in response to experience.
In order to re-establish brain functions that have been lost in the massive nerve-cell die-off that follows an extraordinary event such a stroke, it's necessary to restore lost synapses and form new ones at a rapid pace. It's also important to retrain surviving circuits to take over functions formerly served by lost circuits — this is the basis of rehabilitation therapy.
The rest at the link.

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