Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 34,080 posts. Searching is done in the search box in upper left corner. I blog on anything to do with stroke. DO NOT DO ANYTHING SUGGESTED HERE AS I AM NOT MEDICALLY TRAINED, YOUR DOCTOR IS, LISTEN TO THEM. BUT I BET THEY DON'T KNOW HOW TO GET YOU 100% RECOVERED. I DON'T EITHER BUT HAVE PLENTY OF QUESTIONS FOR YOUR DOCTOR TO ANSWER.
Changing stroke rehab and research worldwide now.Time is Brain!trillions and trillions of neuronsthatDIEeach day because there areNOeffective 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.
So success. How many fucking decades before this gets to your hospital? Probably after your children and grandchildren are dead. THAT is how fossilized I know stroke leadership is.
Study used the GyBAR, a backpack-like prototype portable robot, to
investigate the hypothesis that the balance of both healthy and chronic
stroke subjects can be augmented through moments applied to the upper
body. Gyroscopic actuators are appealing for wearable applications due
to their ability to provide overground balance support without
obstructing the legs. Two experiments involving a different set of
balancing tasks were performed. Experiment 1 compared different
candidate balance-assisting controllers with 10 healthy subjects in a
walking task, and Experiment 2 explored both walking and standing
balance in 5 healthy subjects and 5 individuals with chronic stroke.
Balance performance was measured in terms of each participant's ability
to walk or remain standing on a narrow support surface oriented to
challenge stability in either the frontal or the sagittal plane. By
comparing candidate balance controllers, it was found that effective
assistance did not require regulation to a reference posture. A
rotational viscous field increased the distance healthy participants
could walk along a 30-millimeter-wide beam by a factor of 2.0, compared
to when the GyBAR was worn but inactive. The same controller enabled
individuals with chronic stroke to remain standing for a factor of 2.5
longer on a narrow block. Due to its wearability and versatility of
control, the GyBAR could enable new therapy interventions for training
and rehabilitation. Descriptor Terms: AMBULATION,
ASSISTIVE TECHNOLOGY, BODY MOVEMENT, EQUILIBRIUM, MOBILITY AIDS,
MOBILITY IMPAIRMENTS, POSTURE, REHABILITATION TECHNOLOGY, ROBOTICS,
STROKE, TASK ANALYSIS.
Citation: Lemus, Daniel , Berry, Andrew ,
Jabeen, Saher Jayaraman, Chandrasekaran , Hohl, Kristen , van der Helm,
Frans C. T. , Jayaraman, Arun , Vallery, Heike. (2020). Controller synthesis and clinical exploration of wearable gyroscopic actuators to support human balance.
Scientific Reports, 10(1), Pgs. 10412. Retrieved 8/18/2020, from REHABDATA database.
Is your hospital too fossilized to even try this prior to human trials? Or do you have time to wait five years when your dementia is full blown? Up to you to decide.
There is no cure for Alzheimer’s
disease. Although a few drugs manage temporarily certain cognitive
symptoms of the illness, none can stop or meaningfully slow its
progression. “We really don’t have much to offer people,” says Shannon
Macauley, a neuroscientist at Wake Forest School of Medicine. Virtually
all new treatments have failed in clinical trials. But new research is
looking beyond drugs to see what relief might come from a simple LED
light and a speaker.
Bathing
patients in flashing light and pulsing sounds both tuned to a frequency
of 40 hertz might reverse key signs of Alzheimer’s in the brain,
according to a paper published in Cell on Thursday. “I think
it’s an absolutely fascinating paper to be honest,” says Macauley, who
was not involved in this work. “It’s a very provocative idea. It’s
noninvasive and easy and low cost, potentially, so if it were to come to
fruition in humans—that’s fabulous.”
Still, all this is a big if, Macauley acknowledges. The work was done
in mice with genetic alterations that doomed them to develop key
symptoms and pathology of Alzheimer’s disease. One batch of mice formed
neurofibrillary tangles inside their neurons—dysfunctional knots of a
protein called tau that can lead to the cell’s death. Another batch of
the mice developed amyloid beta plaques—sticky heaps of protein that dam
the flow of communication between neurons. All the mice also had a
third hallmark of the disease—irregular brain activity in the gamma
range of brain waves that oscillate between 30 and 100 times a second.
In 2015 neuroscientist Li-Huei Tsai, director at The Picower
Institute for Learning and Memory at Massachusetts Institute of
Technology, was working on an experiment to manipulate that brain
activity by flashing a white light at these mice. Like light strobes,
our brains flicker. Brain waves are generated when large groups of
neurons oscillate on and off together. Neurons encode our thoughts and
actions and senses in this rhythmic electrical flutter. So when Tsai
tuned her light to flash 40 times a second, or 40 hertz, and flickered
it at the mice, their brains flickered back—generating gamma waves at a
corresponding 40 hertz. Then, something unexpected happened.
When Tsai dissected the mice brains afterward, the amount of amyloid
plaques and tau tangles in the mice that saw the light had plummeted.
“It was the most remarkable thing,” Tsai says. “The light flicker
stimulation triggers a tremendous microglia response. These are the
brain’s immune cells that clear cell debris and toxic waste including
amyloid. They’re impaired in Alzheimer’s disease, but [the light] seems
to restore their abilities.”
This clearing-out process only happened in the visual cortex where
the brain processes light information. To get these effects to penetrate
deeper into the brain, she added a clicking sound like a dolphin’s
chirrup that also had a 40-hertz frequency. When the mice sat in a room
with both the flashing light and the droning sound for an hour day,
seven days in a row, amyloid plaques and tau tangles began falling in
not just the audio and visual cortices but the prefrontal cortex and the
hippocampus as well. “This was one of the big jumps in the new paper,”
Macauley says. “These are the learning and memory centers of the brain.
And there was about a 40 or 50 percent decrease in amyloid and tau
levels. It’s an absolutely impressive feat.”
That showed when Tsai put the mice through a set of cognitive tests.
In one, where the mice were given a familiar and an unfamiliar object to
explore, mice that didn’t get the treatment acted as though they’d
never seen the familiar object. “That shows some memory problems,” Tsai
says. Mice that saw the light and heard the sound spent about two thirds
of the time that untreated mice did examining the familiar object. “It
was unbelievable,” Tsai says. “This is the first time we’ve seen that
this noninvasive stimulation can improve cognitive function. It’s not a
drug or an antibody or anything, it’s just light and sound.”
One possible explanation for this is brains with Alzheimer’s have
irregular, often hyperactive, neurons, says Jorge Palop, a neurologist
at the University of California, San Francisco, who did not work on the
study. By providing the brains with a steady and regular beat, the
repeating light and sound might work as a kind of metronome for brain
activity. “This could be like resetting the mice every day and
correcting some of this abnormal activity that they have,” he says.
“Then downstream of that are all these beneficial effects.”
All of this is still at the level of speculation. Researchers simply
do not know why these brain waves, specifically ones rising from light
and sound stimulation at 40 hertz and no other frequencies, can lead to a
reversal of Alzheimer’s disease symptoms. “That’s a mystery,” says
Terrence Town, a neuroscientist, at the University of Southern
California who was not involved with the work. It’s also not clear if
these beneficial effects would appear or if 40 hertz is the “magic”
frequency in humans, he says.
Tsai is already working on answering those questions. In human
studies underway at Cognito Therapeutics, a start-up she founded with
her colleague Ed Boyden, she says light and sound seem to increase gamma
waves in healthy participants without negative side effects. “Nobody
gets sick or even complains about it,” Tsai says. “But to see a
[therapeutic] effect in humans, you’ll have to wait a long time. If this
approach has an impact, the experiment could easily take five years to
have some conclusive answer.”
I'm sure your doctor will put this in your diet stroke protocol, except use dark chocolate. For all the benefits of dark chocolate in these 7 posts and these 56 on red wine. If your doctor hasn't anything specific and good to say about red wine and dark chocolate you don't have a doctor, you have a fossil of a doctor, fire them. I would skip the heating of the wine and just drink it direct.
Place the dates and the red wine in a small saucepan. Warm the wine
until it’s just hot to the touch and then turn off heat. Allow the dates
to soak for 20 minutes.
Purée the dates together with the red wine until they’re smooth.
Stir in the cocoa powder. Allow the mix to cool.
While the mix is cooling, temper to chocolate chips together with the coconut oil.
Pour this mixture over the interior walls of the chocolate mold,
coating every crevice. You may need to pour the chocolate back out and
pour it in again to make sure all surfaces are covered. You will still
have chocolate left over to pour over the bottom of the chocolates.
Allow the chocolate to harden.
Scoop the date-wine filling into a piping bag or a zip-seal bag. Cut the tip off and pipe the mixture into the prepared molds.
Allow the filling to firm up a little bit in the refrigerator.
Pour the remaining chocolate over the bottom of the molds.
Set them in the refrigerator to firm up before you eat them.