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.

Friday, June 13, 2014

Young Blood Revitalizes the Aging Brain

This may be in mice but what the hell is the downside of getting young blood transfusions? Ask your doctor, and not politely. Your doctor just needs to figure out what a 3 month old mouse would correspond to in humans. Are your doctors even thinking about your cognitive needs at all?
http://brainblogger.com/2014/06/13/young-blood-revitalizes-the-aging-brain/
Aged mice exposed to young blood for five weeks showed a significant increase in the number of cells in the hippocampus, a structure important for learning and memory, positive for signaling molecules (including Erg-1, c-Fos, and pCREB) important for learning processes. In addition, these aged mice showed a significantly increased number of dendritic spines, portions of brain cells that receive signals in order to help transmit information, in the dentate gyrus of the hippocampus.

More at link, including references.
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