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, May 6, 2011

Acute stroke treatment options - Cleveland clinic answers

I asked this question at the clevend clinic chat.

Which of the following is considered to be some of the best possibilities for acute therapy? And who is testing them in clinical trials? - anti-depressants, tumeric, stopping glutamate cell death, niacin, potassium,Irish coffee injection(caffeinol), xenon gas,Sigma-1 receptors,fish oil,marijuana, sensation stimulation, etanercept, caffeine, sleep, nicotine, alcohol, hypothermia, inosines and NEP1-40, SB623, tocotrienols, cardiac glycosides, SK3 channels and nWASP,snake venom, bat saliva
The answer, at least this doctor knew what he was talking about.

Dr__Gabor_Toth: Many of the above agents have been tried in cell cultures, animal models or less frequently humans. Results were many times controversial (antidepressants), potentially beneficial (potassium), indeterminate (caffeinol, desmoteplase bat saliva), or no clear benefit was seen (ancrod snake venom). Some agents/drugs have shown promising results in the lab, but no human trials have been conducted or completed yet (turmeric, niacin, xenon, NEP1-40).

another question
oc1dean: Could liposomes become the transport of choice to get past the blood-brain barrier?
Dr__Gabor_Toth: Although liposomes and basic science research are not my areas of expertise, but I have heard of animal studies using liposomes for potential stroke therapy. It usually takes time from animal models to go to clinical trials. If the animal dara are promising and the method/drug appears safe, human trials can be initiated in the future.
Cleveland_Clinic_Host: Thank you for joining us today. Dr. Toth's chat today is discussing acute stroke treatment options. If your question is directed toward chronic stroke care, recovery and rehabilitation, and most of them could be better answered by a PM&R (rehabilitation) physician, who specializes in stroke recovery.
I wish the host would have just said that no one knows how to help a chronic patient. The  PMR doctors I have seen knew absolutely nothing for either acute or chronic rehab.

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