Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
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Why aren’t robotic arms more common? Asking those who help power chair users with limited upper mobility
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Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
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Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed.
Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
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Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
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Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
Welcome to the r/spinalcordinjuries subreddit, a community for discussing, sharing, and providing support for individuals affected by Spinal Cord Injuries (SCIs). It’s important to note that this subreddit focuses specifically on SCIs and not general orthopedic or spinal issues. Although we encourage asking questions and sharing, please refrain from posting medical questions. Instead, please seek advice from a qualified medical professional to address any issues or concerns you may have.
Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
Focusing on issues facing people with MS and their family and friends. Conversations about support, research, drug therapies, nutrition, exercise, and more.
Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
A group for people with the genetic disease spinal muscular atrophy and their friends and family. Share stories, advertise events, discuss equipment, ask questions - anything goes.
Why aren’t robotic arms more common? Asking power chair users with limited upper mobility
/r/MuscularDystrophy is a forum for users to share resources and experiences related to Muscular Dystrophy.
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
Make the world of people with disability a little bit better by participating in small research surveys. If you like filling out forms and providing information about your life, this is the place for you.
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
/r/MuscularDystrophy is a forum for users to share resources and experiences related to Muscular Dystrophy.
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
A group for people with the genetic disease spinal muscular atrophy and their friends and family. Share stories, advertise events, discuss equipment, ask questions - anything goes.
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
World's Largest Cerebral Palsy Community. Join the active and friendly support chat! https://discord.com/invite/u5Gj6UXTJ4
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
A sub all about chairs on wheels. Here you can discuss your wheelchair, experiences, anecdotes and sob stories, purchase tips, wheelchair sports, accessibility concerns, pitfalls, tips, pictures, wheelchair concepts, travel advice, etc.
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
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Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
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Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
Welcome to the r/spinalcordinjuries subreddit, a community for discussing, sharing, and providing support for individuals affected by Spinal Cord Injuries (SCIs). It’s important to note that this subreddit focuses specifically on SCIs and not general orthopedic or spinal issues. Although we encourage asking questions and sharing, please refrain from posting medical questions. Instead, please seek advice from a qualified medical professional to address any issues or concerns you may have.
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed.
Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
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Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
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Anyone here use (or know someone who uses) a power wheelchair and find it hard to grab stuff?
A place for all those living with the complex and poorly understood functional neurological disorder.
Anyone here use a power wheelchair and find it hard to grab stuff?
Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder. The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles (myotonia) and rigidity.