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.

Wednesday, February 24, 2016

Stroke Patients’ Speech Loss Linked to Loss of Brain Interconnections

The solution to this problem would be enhancing the axon pathfinding and neurite outgrowth. But because we have NO stroke leadership or strategy no one will be looking for these solutions. You as a stroke survivor are fucking screwed for as long as we have craptastic stroke leaders.
http://www.alphagalileo.org/ViewItem.aspx?ItemId=161318&CultureCode=en

Imaging Reveals Disruption of Language Network “Structural Hubs” Directly Associated with Aphasia Following Stroke, Reports Restorative Neurology and Neuroscience
When brain regions that control speech and reading comprehension are destroyed due to blockage of blood flow, patients are often unable to speak or comprehend spoken or written language. These difficulties with language, or “aphasia,” are a common symptom in the aftermath of stroke. However, in a new study published in Restorative Neurology and Neuroscience, researchers report that damage to the underlying connections among different areas of the brain can also affect the severity of aphasia.
The brain’s macro architecture of connections can be reproduced as a “connectome” composed of nodes representing various regions of the brain and their edges, the connections between such nodes. Some of these nodes function as hubs, which are fundamental to the overall organization and distribution of information throughout the brain. When a network hub has an excess of interconnections, it is part of a so-called “rich club network.” There is a growing body of evidence that damage to this rich club network can impair various speech and reading functions in much the same way as direct damage to brain regions normally associated with speech and comprehension.
This investigation involved 44 patients who had experienced a left hemisphere ischemic stroke at least six months prior to the study. Aphasia testing used the Western Aphasia Battery, which determined overall aphasia severity, as well as sub-assessments of speech fluency, auditory comprehension, speech repetition, and naming. Each participant was assigned an Aphasia Quotient (WAB-AQ) as a measure of severity. MRI Diffusion Tensor Imaging (MRI-DTI), which can map the interconnections between brain regions, was used to identify the rich club network in each individual patient.
Investigators found that when imaging revealed that the post-stroke patients studied had different distributions of rich club nodes, their aphasia could differ markedly. They present a striking example in which two patients had similar volumes of stroke damage but very dissimilar numbers of rich club nodes remaining nearby. Patient B had more severe aphasia (lower WAB-AQ = 23.6) than patient A (WAB-AB = 64.6).
“Subjects whose spared cortical language regions are integrated into the remaining network as rich club nodes are less likely to have more severe forms of aphasia,” explained lead investigators Ezequiel Gleichgerrcht, MD, PhD, and Leonardo Bonilha, MD, PhD, from the Department of Neurology, Medical University of South Carolina.
While clinical practice has often focused on the direct damage to the grey matter of the brain, new mapping techniques such as MRI-DTI can examine the white matter connections throughout the brain. The investigators stressed that, “These findings further highlight the potential relevance and utility of mapping the neural connectome of individual subjects. Identifying patterns of white matter integrity has the potential to add valuable information to the well-established volume-based analysis of clinical, neuropsychological, and language outcomes from both theoretical and clinical perspectives.”

Attached files

  • Two representative participants were drawn from our sample to demonstrate the relationship between number of rich club nodes in each hemisphere and language performance. Despite comparable lesion volumes (A = 5796 voxels, B= 5614 voxels) and number of right-hemisphere rich club nodes, patient B – who had one isolated left-hemisphere rich club node – showed remarkably low language performance compared to patient A, who had fourteen nodes participation in the rich club on the left hemisphere.


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