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, July 18, 2016

Imaging technology allows 3-D visualization of Alzheimer’s-related plaques

Your doctor should be following this up so you have a baseline measurement before you get dementia/Alzheimers.
1. A documented 33% dementia chance post-stroke from an Australian study?   May 2012.
2. Then this study came out and seems to have a range from 17-66%. December 2013.
3. A 20% chance in this research. 
  July 2013.

If you have anything close to a decent doctor a protocol will already be in place to prevent this from occurring.   

 
http://medcitynews.com/2016/07/imaging-visualization-alzheimer/?utm_source=hs_email&utm_medium=email&utm_content=31759017&_hsenc=p2ANqtz-9xRPeh25C-cuRq1WVy5tXJWE84eeVzTZXtOVLYArknaDLUeLJd1wdF44JRsmGuBun4dJuY_5ixWY1ujIdL5TvonMojIw&_hsmi=31759017
A nonprofit dedicated to finding a cure for Alzheimer’s disease is funding a new technology that allows greater visualization of amyloid plaques as well as other Alzheimer’s markers, such as tau proteins and vasculature and microglia activation.
The technology was created by scientists at the New York City-based Fisher Center for Alzheimer’s Research Foundation and described in a study published in the scientific journal Cell Reports. Dr. Marc Flajolet, lead author of the study and team leader, said the new technology platform allows the visualization of those markers in larger, three-dimensional amyloid patterns (TAPs) in greater volume. Fisher Center scientists conducted their research on brain tissue from mice and frozen human brain samples of deceased Alzheimer’s patients.
“We are proud that the funding we provide has resulted in innovative, never- before-seen imaging of what causes Alzheimer’s disease,” said Kent Karosen, Fischer Center president and CEO. “The Fisher Center scientists are working diligently to better understand the cause and cure of the disease and with the ability to visualize the causes of Alzheimer’s, we’re one step closer to a cure.”
Flajolet said the Fisher’s team employed the “iDISCO” visualization method involving targeted molecular labeling, tissue clearing and light-sheet microscopy.
The new technology allows 3-D visualization in five different brain regions, better mapping and automated detection enabling faster quantification of plaques, which Flajolet characterized as a cheaper alternative to standard beta amyloid plaque labeling.
“Now we can look at much bigger volumes and see bigger structures that we could not see before in higher resolution,” he explained. “Before this, there were more limitations. We were unable to get the detail we get now.”
He said the technology may open doors of possibility for further Alzheimer’s research that might lead to new Alzheimer’s disease classifications.
“What we have discovered is that amyloid plaques (the groupings of protein that mark the presence of Alzheimer’s) organize themselves into strange patterns that are distributed in different ways, in some cases layers of plaques,” he said. “We don’t yet understand the meaning. But if we could organize patients by how those plaques presented themselves in the brain through retrospective studies and learn the symptoms those patients expressed, we might find ways to categorize stages of the disease differently.”
He said that today, new drugs are tested on Alzheimer’s patients without regard to the level or patterns of plaque in their brains.
“But perhaps, like depression or schizophrenia, not all patients respond to the same drugs. Could it be the same for Alzheimer’s?” Flajolet wondered. “If we are dealing with brains and we know patient symptoms, there is a chance we could propose some categories so the next clinical trial might be used on different patients expressing different patterns. It might only work on 10 percent of patients, but it could open doors.”
The Fisher Center for Alzheimer’s Research Foundation was established in 1995 by philanthropists Zachary Fisher and David Rockefeller. Paul Greengard, who leads the research center, is a Nobel Prize-winning scientist, leads a team of 50 researchers seeking a cure for Alzheimer’s.
Here’s a video from the Fisher Center demonstrating the visualization:


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