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, May 3, 2011

snake venom and stroke rehab

Lets just try all the noxious items on strokees.
http://www.chron.com/disp/story.mpl/metropolitan/3774779.html
The mouths of vampire bats and Malaysian pit vipers are like potentially lethal chemistry sets, dispensing life-taking and life-saving substances.
The vampire bat, a native of Central and South America, feeds exclusively on blood. Its saliva contains a substance that stops the prey's blood from coagulating, so it flows freely. Vampire bats need to consume at least two tablespoons of blood each day.
The viper, a native of Southeast Asia, also is equipped with a sophisticated hemotoxin, a chemical that kills prey by causing its blood to stop coagulating. When the viper bites a rat, the rat suffers a massive hemorrhage and quickly bleeds to death.
"These chemicals are very powerful and very complex, and the animals use them to survive. We are using them to help people survive strokes and lessen the damage they do," said Dr. David Chiu, a neurologist and medical director of the Eddy Scurlock Stroke Center at the Methodist Neurological Institute in Houston.
Chiu is chief of a clinical trial testing the effectiveness of the two venoms on patients who have suffered strokes, which happen when bloodflow to a region of the brain is obstructed. If enough time lapses without treatment, brain tissue dies and death results.
Strokes (most of which are caused by arterial blockage) are the No. 3 cause of death in the United States, killing almost 163,000 people each year. About 700,000 Americans suffer new or recurrent strokes annually.
The drugs Chiu is testing are for emergency use, not prevention of strokes. The sooner a stroke victim receives a powerful anticoagulant to open the obstruction and restore bloodflow, the more likely the patient is to survive and suffer less disability.
"We can't waste time," Chiu said. "Time is brain."
From the clot-busting agent found in the saliva of vampire bats, researchers have genetically engineered a medication called Desmoteplase. Development of this drug is especially exciting for Chiu because it can effectively be administered to a patient up to nine hours after the first symptoms of a stroke appear.
The other trial involves Viprinex, which is derived from a compound called ancrod found in the venom of the Malaysian pit viper. Chiu and his colleagues hope to determine if ischemic stroke victims treated with a one-time dose of Viprinex will experience improved neurological function.
At present, the only clot-busting medication with U.S. Food and Drug Administration approval is t-PA (tissue plasminogen activator), but it must be administered within three hours of the first symptoms.
Chiu hopes to test the drugs on at least 1,000 patients, and expects the trials to last for at least two years. Both studies are random, double-blind, placebo-controlled clinical trials.

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