Recognize symptoms of motor nerve disease that cannot be cured
Motor nerve disease is a group of conditions in which damage to the motor nervous system is progressively produced. This rare disease occurs when nerve cells in the brain and spinal cord called motor neurons do not function properly. Amyotrophic lateral sclerosis (ALS) is one of the most common types of motor neuropathy in adults.
Motor nerves are the parts of the body that control important muscle activities such as walking, talking, grasping, breathing, and swallowing. The importance of this nerve in the movement of the human body means that motor neurological disease can have a major impact on daily life. People with motor nerve disease are becoming increasingly limited in their activities.
A common type of motor nerve disease is amyotrophic lateral sclerosis (ALS). Therefore, motor nerve disease is often identified and referred to as ALS. This disease, also known as Lou Gehrig, usually affects adults over 40, especially more than 60, and is slightly more prevalent in men than women. About 1 in 20 people with this disease have family members with a history of motor disease or frontotemporal dementia, a rare type of dementia that is characterized by abnormalities in the front and sides of the brain. But the cause of motor nerve disease in general is often not detected with certainty.
Be aware of various symptoms of motor nerve disease
Motor nerve disease causes disorders of the motor nervous system, called the upper motor neurons (UMN) and lower motor neurons (LMN). Muscle cannot function properly if there is a signal disturbance between LMN and muscle. This can then gradually weaken the muscles and cause uncontrolled contractions. Meanwhile, if there is a disturbance between the nerve parts of UMN and LMN, it can cause muscle stiffness and body movements to become severe and slow. Eventually, the body's ability to control movement will gradually disappear.
ALS is the most common motor nerve disease in adults with symptoms of muscle contraction, muscle stiffness, atrophy or loss of muscle tissue, and progressive weakness of skeletal muscle.
People suspected of having ALS should immediately consult a neurologist or neurologist. Note the emergence of ALS symptoms that are usually in the form shown below.
Initial symptoms
Further symptoms:
The above symptoms do not appear suddenly, but gradually, over several weeks and months, starting with one side of the body.
ALS symptoms that are felt by everyone are sometimes difficult to diagnose because they may resemble the symptoms of other diseases. To detect this disease, physical and neurological examinations such as strength of limbs, coordination and balance, hearing and speech, vision, sensory abilities, mental states, and changes in behavior and mood are needed. Studies to assess nerve function, cerebrospinal fluid analysis, and blood tests will also be needed to determine the causative factor.
In fact, there is currently no cure for motor nerve disease. Manipulation that can be sought at this stage is only to relieve symptoms so that daily activities are not interrupted. In the final stages, symptoms of motor nerve disease can make it difficult for patients to perform various basic bodily functions such as breathing, and must be assisted in almost every daily movement.
If this has affected the respiratory muscles, this condition can cause respiratory failure if it does not receive help. Treatments are designed to give patients a better quality of life, feel comfortable and adapt to the progressive loss of bodily functions such as swallowing, breathing, communication and movement.
Motor nerves are the parts of the body that control important muscle activities such as walking, talking, grasping, breathing, and swallowing. The importance of this nerve in the movement of the human body means that motor neurological disease can have a major impact on daily life. People with motor nerve disease are becoming increasingly limited in their activities.
A common type of motor nerve disease is amyotrophic lateral sclerosis (ALS). Therefore, motor nerve disease is often identified and referred to as ALS. This disease, also known as Lou Gehrig, usually affects adults over 40, especially more than 60, and is slightly more prevalent in men than women. About 1 in 20 people with this disease have family members with a history of motor disease or frontotemporal dementia, a rare type of dementia that is characterized by abnormalities in the front and sides of the brain. But the cause of motor nerve disease in general is often not detected with certainty.
Be aware of various symptoms of motor nerve disease
Motor nerve disease causes disorders of the motor nervous system, called the upper motor neurons (UMN) and lower motor neurons (LMN). Muscle cannot function properly if there is a signal disturbance between LMN and muscle. This can then gradually weaken the muscles and cause uncontrolled contractions. Meanwhile, if there is a disturbance between the nerve parts of UMN and LMN, it can cause muscle stiffness and body movements to become severe and slow. Eventually, the body's ability to control movement will gradually disappear.
ALS is the most common motor nerve disease in adults with symptoms of muscle contraction, muscle stiffness, atrophy or loss of muscle tissue, and progressive weakness of skeletal muscle.
People suspected of having ALS should immediately consult a neurologist or neurologist. Note the emergence of ALS symptoms that are usually in the form shown below.
Initial symptoms
- Difficulty graspng objects or lifting objects because of weak hands.
- The foot "falls" due ito ankle muscle weakness.
- Drag your feet.
- Difficult to lift arms because his shoulders are weak.
- It is not clear when we talk.
- Muscle contractions or muscle cramps.
- Difficulty maintaining posture.
- The muscles to talk and swallow begin to interfere, this symptom is similar to a stroke.
- Respiratory muscle disorders.
- I woke up several times at night because my brain lacked oxygen.
Further symptoms:
- Difficulty moving limbs.
- Stiff muscles and joints can be painful.
- Difficulty swallowing and talking.
- Excessive saliva due to reduced swallowing can cause saliva.
- Excessive yawning even if they don't feel tired.
- Patients often struggle to control their emotions and cry uncontrollably.
- Hard to breathe.
The above symptoms do not appear suddenly, but gradually, over several weeks and months, starting with one side of the body.
ALS symptoms that are felt by everyone are sometimes difficult to diagnose because they may resemble the symptoms of other diseases. To detect this disease, physical and neurological examinations such as strength of limbs, coordination and balance, hearing and speech, vision, sensory abilities, mental states, and changes in behavior and mood are needed. Studies to assess nerve function, cerebrospinal fluid analysis, and blood tests will also be needed to determine the causative factor.
In fact, there is currently no cure for motor nerve disease. Manipulation that can be sought at this stage is only to relieve symptoms so that daily activities are not interrupted. In the final stages, symptoms of motor nerve disease can make it difficult for patients to perform various basic bodily functions such as breathing, and must be assisted in almost every daily movement.
If this has affected the respiratory muscles, this condition can cause respiratory failure if it does not receive help. Treatments are designed to give patients a better quality of life, feel comfortable and adapt to the progressive loss of bodily functions such as swallowing, breathing, communication and movement.
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