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, December 26, 2011

Lab-grown glands, eyes and brain parts

Blogger Mo Costandi helps me understand a lot of the neurogenesis/stem cell work done by research labs.
This one has some great ideas needing followup.
http://www.guardian.co.uk/science/neurophilosophy/2011/dec/04/1
A selected paragraph:
Growing a complete, functioning brain is unfeasible, but there is real potential in growing functional neural tissue containing specific types of cells, for transplantation into the human brain. This is one avenue of research that the team are investigating. Last year, they showed that ES cells can be coaxed to differentiate into functional cerebellar Purkinje cells, which integrate themselves into the brain when transplanted into mouse foetuses.
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