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, August 29, 2017

Why We Must Attack Alzheimer's Disease on a Range of Research Fronts

Stroke doesn't need this, don't you know 'Stroke is Treatable'.  Then why isn't everyone 100% recovered? Whom is lying?






 https://www.rdmag.com/article/2017/08/why-we-must-attack-alzheimers-disease-range-research-fronts?
 by Diane Bovenkamp, Ph.D. BrightFocus Vice President, Scientific Affairs
Alzheimer’s is a frustratingly complex disease of mixed origins that expresses itself in different ways. At least 70 percent of its variation remains unexplained. In an age when so much about Alzheimer’s disease is still unknown, a depth and range of funded topics is a necessity.  Numerous routes of discovery must be explored.
Scientists recognize that it’s unlikely one magic drug will prevent, postpone, or cure Alzheimer’s. Instead, a combination approach, or “cocktail” of different drugs may be necessary to modify or slow the progression of this complicated disease. That makes it all the more important that scientists explore various pathways and stages of the disease to find feasible drug targets.
Alzheimer’s Disease Research (ADR), a program of the BrightFocus Foundation, is currently funding nearly 100 research projects worldwide, an investment totaling more than $22 million.
Here’s an overview of some of the Alzheimer’s topics engaging researchers in that program today.
Stopping Alzheimer’s by understanding how it starts
Our understanding of what causes Alzheimer’s disease remains incomplete, but we learn more each day. We know that a major turning point in the disease is when proteins in the brain—including tau and amyloid beta (AB)—go from “normal” to “diseased” and cause neuron death.  These proteins undergo molecular changes and take on altered shapes, causing them to collect into tangles, plaques, and vascular deposits that are toxic to surrounding tissues.
This picture is complicated by the fact that some neurons will develop tau tangles, while others next to them remain healthy, for reasons we don’t understand. Some researchers are pursuing an exhaustive cell-by-cell comparison, to see what makes some neurons more vulnerable or resistant than others.
Two examples here and here.
Regulating immune factors and clearance mechanisms
One unifying theory about Alzheimer’s disease is that it may be triggered, in part, by a breakdown in the brain’s immune system.  Normally our brain has ways of clearing damaged cells and other unwanted particles and disposing them into the cerebrospinal fluid and bloodstream, akin to “taking out the garbage.” But a chronic rise in unwanted debris, including toxic AB and tau proteins, can short-circuit the immune system.
When cells in the central nervous system, known as microglia, malfunction, they lead to tissue inflammation.  Researchers are looking at what causes the immune response to become unbalanced, and whether there are ways to help the brain’s immune system do a better job of fighting Alzheimer’s.
Two examples here and here.





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