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, January 7, 2020

New York hospital giant gains FDA approval for PET agent to diagnose Parkinson’s

With ANY BRAIN CELLS AT ALL our stroke leaders could see this as a way to objectively see the damage caused by your stroke. Knowing that could then lead to EXACT PROTOCOLS that would address that damage. But never mind, NOTHING WILL OCCUR. 

New York hospital giant gains FDA approval for PET agent to diagnose Parkinson’s

The research offshoot of Northwell Health has scored approval from the Food and Drug Administration for a new imaging agent that can help diagnose Parkinson’s disease.
Fluorodopa F 18, as the drug is called, is injected into patients in preparation for a PET scan. Once administered, the agent helps radiologists to detect any damaged or lost nerve cells in the brain. Clinicians can also use it to follow the disease’s progression, along with the integrity of intracerebral implants.
“This FDA approval is the pinnacle of our venture to have a safe and effective imaging agent for the differential diagnosis of Parkinsonian syndromes,”  Thomas Chaly, PhD, chief of cyclotron/radiochemistry at the Feinstein Institutes for Medical Research, said in a statement.
Chaly, who was instrumental in gaining the FDA approval, added that he hopes PET centers across the United States will begin incorporating Fluorodopa F 18 into their regular protocols alongside other previous methods for diagnosing Parkinson’s. You can read more about the contrast agent here.

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