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.

Tuesday, September 16, 2014

Brains can power up to get around Alzheimer's plaques

This might explain why Bernadette the nun could have a brain full of plaque and still function. And maybe explain the fact that higher blood pressure in the elderly leads to less cognitive decline.
http://www.newscientist.com/article/dn26206-brains-can-power-up-to-get-around-alzheimers-plaques.html?#.VBboYWOVCug
A couple of paragraphs, rest at link.
Jagust found that older people with plaques had increased blood flow – which means stronger activation of that brain area – in the regions of the brain that are usually activated during memory formation, compared with the older people who did not have plaques. The team then analysed whether this extra brain activation might be helping to compensate for the plaques.
And the results were clear. In the case of the older people with beta-amyloid, the more accurate their memory of the picture, the more active their brain had been when they studied the image in the fMRI. "That suggested to us that they were able to ramp up activity to retain more information," says Jagust. "We interpret this as a compensation or plasticity. The older people who didn't have amyloid in the brain did not do it."
This boosting of brain activity seems to be related to the amount of plaques a person had. The more beta-amyloid protein someone had, the more they tended to ramp up their brain activity while memorising the scene. However, this effect tailed off in the people with the greatest amount of plaques. "It suggests this is a transitory phenomenon. Eventually, this sort of compensation becomes lost. And that might be something that happens in the progression to cognitive decline," Jagust says.

The results could also help explain why some people have the plaques without appearing to have dementia. "The fact that brain amyloid is detectable in cognitively normal elderly subjects has been used historically as an argument to support the idea that amyloid may not be as toxic as suggested by experimental studies," says Roger Nitsch, a neuroscientist at the University of Zurich in Switzerland. "This work challenges this view by addressing how elderly subjects can retain normal cognition despite the presence of brain amyloid."

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