When this term "Bradykinesia" first came up on my hospital notes, I confess that I had no real idea what it meant as it was not discussed. I thought that I was just becoming more clumsy at times and left it at that.
This left me struggling to understand just what was going on inside my brain for some time, but after reading this article , from https://www.verywell.com/bradykinesia-2612077. it is all starting to make more sense now.
What is Bradykinesia in Parkinson's Disease?
Slowed Movement That Affects Both Fine and Gross Motor Control
Updated
June 07, 2017
Bradykinesia refers to slowness of movement. It's one of the three characteristic symptoms of Parkinson's disease (tremor and rigidity are the other two). In other words, bradykinesia occurs in everyone who has Parkinson's.
This slowness of movement is
most obvious when a person with Parkinson's is starting or performing activities that
require several successive steps. These can include all kinds of activities of daily life like getting
dressed, making a sandwich, or getting to a doctor’s appointment.
Tasks requiring fine motor
control (buttoning a shirt or using utensils, for example) are particularly
slow for someone with bradykinesia from Parkinson's disease, and reaction times are much slower, as well.Bradykinesia also can cause someone with Parkinson's to shuffle more than walk, and to use slow, short steps. Finally, this problem may lead to soft speech that's difficult for others to understand.
Testing for Bradykinesia in Parkinson's Disease
When your doctor tests for the presence of bradykinesia, she will ask you to perform rapid, repetitive, alternating movements of the hand (such as moving your palms up and down, finger taps, and hand grips).
People who have bradykinesia generally can't move quickly.
The slowness of movement can
manifest in gestures, in speech, and even in how often or how quickly you can
blink your eyes.
Sometimes, bradykinesia is
subtle in a person with Parkinson's disease, especially in the early stages of the
condition.To detect it, doctors look for hesitation before the person starts to move, and for reduced arm movements while walking.
What Does Bradykinesia Feel Like?
When you have bradykinesia due to
Parkinson's disease, you may feel like your body isn't obeying your brain's
commands, at least immediately (the way it used to do).
You may also feel as if your
arms and legs are weak, because they won't do what you want them to do, or your
limbs may ache as you try to perform tasks that involve repetitive motion, such
as walking.
In some people with advanced
Parkinson's disease, bradykinesia leads to a sensation of their feet being stuck to
the floor, because they feel as if they're unable to get them moving. It may be possible to
break this pattern through therapy that encourages you to perform such tasks as
marching in place and stepping over imaginary lines.
You may also have trouble
writing, and notice that your handwriting is getting smaller and slanting upwards to
the right. This is a symptom called micrographia, and it's related to
bradykinesia in Parkinson's disease.
Your emotional state may also
affect your bradykinesia but in a beneficial way.
For example, even if you cannot move due to
your Parkinson's, if someone shouts “fire!” you may be able to get
up and run fast. This is called "kinesia paradoxica."
Fortunately, Parkinson's disease does not
destroy the programs in your brain that allow you to react this way in
an emergency.A Word From Verywell
Although Parkinson's disease can't be
cured, medications and other therapies can help manage the symptoms,
including bradykinesia.
If you're having trouble
accomplishing tasks in daily life because of your Parkinson's disease, talk to
your doctor about treatments that might help stabilize or even improve your symptoms.
Sources:
Frontera, Walter R., J. K.
Silver, and Thomas D. Rizzo. Essentials of Physical Medicine
and Rehabilitation: Musculoskeletal
Disorders, Pain, and Rehabilitation. Philadelphia, PA:
Saunders/Elsevier, 2008. Print.
2013 Feb 15;87(4):267-73.
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I always say that we may have this illness, but we are all so different.
This is my own daily problems, but I would gladly share anyone elses, if they send them in,