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.

Saturday, October 25, 2014

Identification of Mood-Relevant Brain Connections Using a Continuous, Subject-Driven Rumination Paradigm

What is your doctor doing to make sure you aren't ruminating  on the depressing facts that your doctor hasn't given you any hope or pathway to 100% recovery?
http://cercor.oxfordjournals.org/content/early/2014/10/18/cercor.bhu255.abstract
  1. Michael D. Greicius3
+ Author Affiliations
  1. 1War Related Illness and Injury Study Center, VA Palo Alto Healthcare System, Palo Alto, CA, USA
  2. 2Department of Psychiatry and Behavioral Sciences
  3. 3Department of Neurology and Neurological Sciences, Functional Imaging in Neuropsychiatric Disorders (FIND) Laboratory, Stanford University School of Medicine, Stanford, CA, USA
  4. 4Parietal Team, INRIA Saclay, Gif-sur-Yvette, France
  5. 5Interdepartmental Program in Neuroscience, Northwestern University, Evanston, IL, USA
  1. Address correspondence to Michael Greicius, Mail Code 5420, Stanford, CA 94305, USA. Email: greicius@stanford.edu
  1. Anna-Clare Milazzo and Bernard Ng contributed equally.

Abstract

Rumination, an internal cognitive state characterized by recursive thinking of current self-distress and past negative events, has been found to correlate with the development of depressive disorders. Here, we investigated the feasibility of using connectivity for distinguishing different emotional states induced by a novel free-streaming, subject-driven experimental paradigm. Connectivity between 78 functional regions of interest (ROIs) within 14 large-scale networks and 6 structural ROIs particularly relevant to emotional processing were used for classifying 4 mental states in 19 healthy controls. The 4 mental states comprised: An unconstrained period of mind wandering; a ruminative mental state self-induced by recalling a time of personal disappointment; a euphoric mental state self-induced by recalling what brings the subject joy; and a sequential episodic recollection of the events of the day. A support vector machine achieved accuracies ranging from 89% to 94% in classifying pairs of different mental states. We reported the most significant brain connections that best discriminated these mental states. In particular, connectivity changes involving the amygdala were found to be important for distinguishing the rumination condition from the other mental states. Our results demonstrated that connectivity-based classification of subject-driven emotional states constitutes a novel and effective approach for studying ruminative behavior.

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