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, November 28, 2014

Lab Technique May Lead to Better Understanding of the Fatigued Brain

Send your doctor after this researcher to see if this may explain the blasted fatigue most survivors deal with. See page 6.
http://www.sfn.org/~/media/SfN/Documents/Press%20Releases/2014/Neuroinflammation_PressPacket.ashx
Senior Author: Mary Harrington, PhD
Smith College
Northampton, Mass.
(413) 585-3925
mharring@smith.edu
Lab Technique May Lead to Better Understanding of the Fatigued Brain
Animal study shows fatigue from brain inflammation found to worsen with age
A procedure that induces fatigue in mice by activating the immune system has produced new insights into the underlying neural mechanisms that trigger fatigue, a common and often disabling symptom, according to research presented today at Neuroscience 2014, the annual meeting of the Society for Neuroscience and the world’s largest source of emerging news about brain science and health.
“It’s important to have a method to induce fatigue in mice so that we can develop better clinical treatments,” said senior author Mary Harrington, PhD, of Smith College in Northampton, Mass. “With this new procedure, we can now identify the brain cells that generate fatigue in mice and are beginning to map the brain pathways by which inflammation in the brain leads to that fatigue.”
It’s estimated that more than one-third of the workforce in the United States has experienced fatigue lasting longer than two weeks, costing employers more than $100 billion every year. Chronic fatigue is also common in people with neurological disorders. Up to 40 percent of people with Parkinson’s disease and multiple sclerosis, for example, cite fatigue as being the most disabling symptom of their disease.
The procedure developed by Harrington and her colleagues uses the cytokine IL-1 to initiate fatigue in mice without other symptoms, thus allowing researchers to explore the brain pathways related specifically to fatigue. With the procedure, Harrington and her team have recently discovered that the fatigue associated with inflammation within the mouse brain gets worse with age and that it does not require, as was previously suspected, a reduction in the activity of orexin neurons, which play a big role in keeping the brain alert and awake.
Research was supported with funds from the National Institute of Nursing Research.
Scientific Presentation: Tuesday, Nov. 18, 11 a.m.–noon, Room 147B

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