My therapy seems to continue 24 hours a day. There is nothing here that
is clinically proven but I believe that even minimal tries every day
will eventually produce neuroplastic change.
This knowledge came from reading lots of books, mostly Stronger After
Stroke by Peter Levine. Everything I do has to be looked at in terms if
it will help my recovery. I'm left side affected with at least half of
my motor cortex dead and all of my pre-motor cortex dead, no real damage
to my sensory cortex. This diagnosis did not come from my doctor since
he never even showed me my MRI, I figured this out myself by joining a
research study that did an fMRI scan on my brain. My sensory cortex
supposedly was not affected but is less than before so I am assuming
that it was routed thru the motor cortex across the central sulcus to
get to the correct nerve endings. And since the motor cortex is mostly
dead I have to find a new pathway to those nerves. This is rather
depressing that I have to do all this self-diagnosis myself.
Since I am 4 years out I am way past the normal spontaneous recovery of
the penumbra of the stroke. This means that all the work I am doing is
to neuroplastically move control of dead areas to another location in
the brain. The concept I am working on is to at least get some movement
by passively moving body parts that don't work. Passive movement does
have some research backing it up. http://www.ncbi.nlm.nih.gov/pubmed/15003755
Normal day, going to work.
Breakfast is pretty much a one-handed affair. I don't have finger
extension yet to be able to hold my bowl of cereal with my left hand. I
can't keep my arm on the table due to spasticity constantly pulling it
off, My OT tried to use opening the refrigerator door with my left hand
as a therapy goal but since the fingers still haven't opened that one is
still a failure. Zipping up a coat is still a challenge with the
limited pinch grasp I have. I walk 2 blocks to the bus stop with my
cane. I use a cane to get to work because the Messenger bag I carry
pulls me off balance. At the corner waiting for the bus I lift my left
foot up to the top of an 18 inch high rock. this mimics the stair
stepping my PT always had me doing.After that I stand on my right leg
and pull my left leg back until it rests on my left toes, this is trying
to get my hamstring to fire. Then comes standing on my left leg and
stepping back and forth with the right leg, good for all the little
muscles that fire in your legs to keep you balanced, if necessary I use
the cane in my right hand for balance. This came from a Tai Chi class I
took. I add using my cane for PROM movements of my shoulder. On the bus
ride itself I have to decide if I should work on keeping my arm
straight, trying to stop the spasticity in my bicep, or flex my fingers
open and closed with my good hand.
At work, I use my good hand to guide me bad hand with a single finger
pointing down to type. Sitting in my work chair I pull my left leg under
me, trying to fire my hamstring muscles.I try to dangle my arm over the
side of the chair to let it know that it can relax and hang straight.
Washing my hands at the sink I have to open and close the single lever
faucet with my bad arm/hand. Then I go to the stairwell and do a set of
50 toe raises.
Waiting at the bus stop at night I raise and lower my lower arm 50
times. Next is knee bends on the left side, just going down enough to
unlock the knee and then straightening it out again. On the way home I
stop at one of our apple trees in our yard and put the affected hand
around a limb that is at shoulder height, push and pull with the
biceps/triceps. Sitting on a couch reading requires either sitting on my
flattened hand or keeping the whole arm straight next to my leg.
While sitting I rotate my arm outward from my leg, even if it is only 3 inches at a time.
Eating at the table I just put my left hand flat on the table next to my
plate, just trying to keep it in one place is a workout quieting down
my spastic pectoralis and bicep muscles. I sneezed once at the table and
swept all my dishes to the floor, so now I grab my affected hand as
soon I notice a sneeze coming. In the shower at night I put my affected
hand directly
under the shower head trying to stimulate the sensations. This idea
came from Sensory Re-education of the Hand After Stroke by Yekeutiel,
Margaret. I also have a small fingernail brush that I use on my affected
hand. The other trial I work on is hot and cold water on the hand from
http://myweb.ncku.edu.tw/~fzshaw/ ASA.pdf
Researchers found that cycles of heat and cold significantly enhanced the
sensory and motor function in the arms and hands of stroke survivors after a few weeks of therapy.
At night I have to decide if I want to sleep on my back which requires
putting my affected fist under my butt, or sleep on my side with my
affected hand flattened out under my pillow.
Other therapies during a regular day. Riding in a car means either
flexing my fingers of my affected hand or straightening my left arm and
just holding it straight.
Every time I stop walking I have to consciously tell my left arm to
relax and hang straight by my side. This is rather embarassing for a guy
walking around to have his bent arm constantly banging into his crotch.
As much as possible I try to come up with exercises that engage my
triceps to keep my arm straight. I also work on exercising my biceps
because exercising spastic muscles does not increase spasticity as your
therapist probably told you.
None of this is intended to be medical advice, Just my opinion that if
you are going to recover you need to consider it a constant job, either
with exercises or mental imagery of those exercises.
My suggestion is that you take whatever movement you do have and work at the outer limits of that movement.
What I have to do is think every single moment of the day if there is
some movement I should practise or should I be thinking about that
movement. What this means is that I have to do everything the hard way
to get to recovery rather than compensatory movements.
This book, The survivors club : the secrets and science that could save
your life / Ben Sherwood, was interesting in that it broke down
survivors of disasters into 3 groups. 10% would actively become leaders,
80% would follow the leaders, 10% would do nothing. I try to apply this
to my stroke survivorship and am working on being in the top 10%.
In further posts I will detail the work I do for rehab.
No rest for the wicked.
Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 28,972 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 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.
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