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, August 24, 2012

Virus could aid post-stroke recovery

Another option needing more research. More down under brains.
http://www.odt.co.nz/campus/university-otago/223084/virus-could-aid-post-stroke-recovery
In a remarkable twist, a virus which causes scabby mouth skin infection in sheep could be used to help people recover better after strokes, new University of Otago research suggests.
Marie Inder, who will graduate from Otago University today with a PhD in microbiology and immunology, said the research, at the university's virus research unit, could create "exciting new options" for medical treatment.
Those included potentially improved recovery from some strokes, by increasing the repair of blood vessels in the brain.
After her own father, Robert Inder, survived a stroke in 2004, she had become more aware of the need to improve post-stroke therapies.
A growth factor protein generated by the virus could also potentially be used in other therapeutic settings, including to improve healing of diabetic skin ulcers and burn injuries.
Ms Inder devoted her doctoral studies to analysing the growth-factor protein- called "vascular skin growth factor" (VEGF). This promotes skin and blood vessel development.
The growth factor is generated by the orf virus, using hijacked host cells.
The orf virus causes scabby mouth in sheep, and a skin infection in humans.
In order to generate the protein growth factor by using hijacked host cells, the virus uses a gene it had earlier "stolen" from its hosts hundreds of thousands of years ago.
The virus replicates only in growing host skin cells, and uses the VEGF protein to promote positive conditions for its own development.
An unusual aspect of this particular growth factor is that it stimulates skin growth without promoting an inflammatory response.
This could help in therapeutic uses, including wound healing.
Ms Inder, who is of Samoan ancestry, said she was "really excited and really relieved" to have completed her research, which was supported by an HRC Pacific Health PhD Scholarship.
Andrew Mercer, who is director of the microbiology department's virus research unit, has said some viruses deployed "a vast array of weapons".
By enlisting aspects of the viruses' strengths to work for humans rather than against them, "a whole new arsenal of tools" could be created to counter diseases.
Prof Mercer, who supervised Ms Inder's research, with fellow supervisors Dr Lyn Wise and Dr Stephen Fleming, said her research had contributed significantly to the field.

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