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, September 22, 2017

Can Alzheimer's be stopped years before it starts?

And if we had a great stroke association we could bring together hundreds of institutions together to dole out problems in stroke to solve. But we have fucking failures of stroke associations instead sucking up money that could be put to a better use.  If a vaccine is developed then all stroke survivors should probably get it due to our likely descent into dementia.
https://medicalxpress.com/news/2017-09-alzheimer-years.html?
September 15, 2017 by Erica Rheinschild 
Researchers at the Keck School of Medicine of USC are tackling the sixth-leading cause of death in the United States—Alzheimer's disease—with a new study that intervenes decades before the disease develops.
The school is joining approximately 90 institutions in North America, Europe and Australia in the Generation Study, which is testing a and oral medication to prevent or delay Alzheimer's in older adults at increased risk for developing the disease. More than 70 USC researchers across a range of disciplines are dedicated to the prevention, treatment and potential cure of Alzheimer's.
By focusing on prevention, the study is taking a different approach to halting a disease that affects 47 million people worldwide.
"One of the challenges in developing new medications for Alzheimer's is that researchers tend to test medications on people with more advanced Alzheimer's, and the medications are simply not proving to be effective," Lon Schneider, the study's lead investigator. "By intervening 10 to 12 years before Alzheimer's manifests, we may be able to stop it before it begins or delay the symptoms."
Adults 60 to 75 years of age with normal cognition who are interested in participating must undergo genetic testing for the apolipoprotein e4 (APOE4) gene, which is associated with an increased risk of developing Alzheimer's.
About half of people with Alzheimer's disease carry the APOE4 gene, which can be inherited from either parent, said Schneider, professor of psychiatry and the behavioral sciences and professor of neurology. About 25 percent of the population carries one copy of the APOE4 gene, and about 2 to 3 percent of the population carries two copies, having received one from each parent. To qualify for the study, participants must have two copies of the gene.
Delay the disease
Qualifying participants may randomly receive either a vaccine, oral medication, placebo vaccine or placebo oral medication. Both the vaccine and oral medication target —the main component in amyloid plaques in the brain and a culprit in Alzheimer's—in two different ways: The vaccine helps the body develop antibodies against amyloid beta, while the oral medication blocks an enzyme that creates amyloid beta. Participants may receive the study medications for five to eight years.
"If we are able to show that the vaccine or oral is effective at delaying Alzheimer's among people at higher risk, then this would strongly imply that we are on the right track for developing treatments," Schneider said. "If we can delay the onset of Alzheimer's by five years, for example, the incidence of the illness would drop by half. It would also give individuals five more years without symptoms of the illness."
Should the vaccine or prove to be effective in people with two copies of the APOE4 gene, then it would likely also be effective for other people at risk for Alzheimer's, according to Schneider.
"Our clinician-scientists have been actively involved in clinical drug development for Alzheimer's for more than 30 years," said Rohit Varma, dean of the Keck School of Medicine. "This study is a reflection of our continued efforts to conquer one of the greatest health challenges of our time."
For information about how to participate in the study, contact Nadine Diaz at (323) 442-7600 or ndiaz@usc.edu.
Provided by: University of Southern California search and more info website
 

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