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, April 18, 2023

A Parkinson’s ‘game changer,’ backed by Michael J. Fox, could lead to new diagnostics and, someday, treatments

Does your competent? doctor know that  this is needed because of your risk of Parkinson's post stroke? 

Your risk of Parkinson's here:

Parkinson’s Disease May Have Link to Stroke March 2017 (Your doctor has had 6 years to put together Parkinson's prevention protocols. Was your doctor competent in doing that?)

A Parkinson’s ‘game changer,’ backed by Michael J. Fox, could lead to new diagnostics and, someday, treatments

NEW YORK — Michael J. Fox was sitting in his Upper East Side office surrounded by Emmys and an Oscar — one he received not for his acting but for his Parkinson’s philanthropy. (“Humanitarian stuff,” he said nonchalantly.) He wore blue trousers and a T-shirt, and Adidas sneakers with no socks. His hair, years ago always perfect, was a bit disheveled, and he was in constant movement in his chair, a hallmark of the Parkinson’s disease that has defined half of his life.

This past year has been particularly difficult for Fox. As he sipped Coke Zero through a straw — drinking is hard with Parkinson’s — the 61-year-old icon recounted how he had broken multiple bones in a fall, including some in his hand and his face.

“It’s been a terrible year,” he said.

But, he added, in some ways he was “feeling better.” He won that Oscar. A new documentary on his life will be coming out in May. And, most importantly, there was the scientific discovery he wanted to talk about.

“This is the thing,” he said. “This is the big reward. This is the big trophy.”

The trophy is science — and specifically research funded by the Michael J. Fox Foundation for Parkinson’s Research that has resulted in the clearest evidence yet that the presence of a particular misfolded protein, alpha-synuclein, can be used to determine if people have Parkinson’s. It is an advance that may soon be used to develop better diagnostics, but more importantly could rapidly accelerate the search for treatments for the disease.

The new findings, published in The Lancet Neurology, are the result of a 1,123-person study that has cost the Fox Foundation hundreds of millions of dollars since it began in 2010. Right now, alpha-synuclein can only be detected by taking a spinal tap, a difficult and uncomfortable procedure. But scientists say they hope that it could be detected in blood, a skin biopsy, or possibly even in a swab of the nose. An editorial in the medical journal called the test “a game-changer in Parkinson’s disease diagnostics, research, and treatment trials.”

The result is convincing in part because of the unique resource of patient volunteers that Fox was able to bring together, said Vikram Khurana, chair of movement disorders at Brigham & Women’s Hospital.

“It is certainly head and shoulders, in my view, the best resource that we have in the Parkinson’s disease research community to really analyze the behavior and molecular and clinical aspects of our patients,” Khurana said.

Fox, who was diagnosed with a very early case of Parkinson’s at age 29, said that he keeps going back to documentary footage of his childhood. At the time, there was no way to know he would develop the disease; soon, he said, a child like that might be able to simply get a nasal swab at 2 or 3 or 4. “It’s all changed. It can be known and treated early on. It’s huge.”

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