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.

Saturday, March 14, 2015

Ribosomes regulate stem cell fate

There is still so much unknown about stem cells that current research seems more like a shot in the dark that any logical way to proceed. This is one of the many reasons that the miracle of stem cells contributing instantly to Godie Howes' recovery is impossible to believe.
http://www.sciencemag.org/content/347/6227/1214.4.full?utm_campaign=email-sci-ec&utm_src=email
The use of stem cells in regenerative medicine holds enormous therapeutic potential. However, scientists still need to fully understand the molecular signals that control the ability of stem cells to self-renew and differentiate. To identify genes that many regulate this, Fortier et al. screened a library of mouse embryonic stem cells (ESCs) containing chromosomal deletions. They found that the loss of a single copy of several genes encoding protein subunits of the ribosome, a large protein complex that translates mRNA into proteins, resulted in impaired ESC differentiation but did not affect self-renewal. 
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