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Motor neuron patients do not necessarily have difficulty breathing, for motor neuron disease, can be carried out with drugs**, usually can be appropriate exercise, enhance physical fitness, improve physical disorders, pay more attention to rest, ensure adequate sleep, pay attention to the health of diet, pay attention to rich nutrition, pay attention to indoor ventilation. However, patients with severe motor neuron disease have difficulty breathing, neuronal disease may cause muscle beating, muscle atrophy, and severe will also cause patients to have dyspnea and shortness of breath.
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Hello, motor neuron disease is a group of chronic progressive degenerative diseases that mainly damage the anterior horn of the spinal cord, the motor nucleus of the cranial nerve and the pyramidal tract. Paralysis caused by upper and/or lower motor neuron damage is the main clinical manifestation, and the combination of upper and lower motor neuron damage is the most common. As long as the patient suffers from this disease, the muscles first atrophy, and finally the patient dies due to the inability to breathe while the patient is conscious.
Therefore, this kind of patient is also called "ALS".
Guidance: At present, this disease is a worldwide problem, and there is no effective method. The dyspnea you mentioned is caused by respiratory muscle atrophy and paralysis, and the problem of swallowing and choking can be solved by giving a lower gastric tube to avoid lung infection caused by repeated coughing.
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In the later stages of motor neuron disease, symptoms such as dyspnea will occur, and it is necessary to follow the doctor's instructions for medication in a timely manner**, which is a group of **unspecified choice** chronic progressive neurodegenerative diseases of spinal cord anterior horn cells, brainstem motor neurons, cortical pyramidal cells and pyramidal tracts.
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Motor neuron disease (MND) is a group of chronic, progressive neurodegenerative diseases of the anterior horn cells of the spinal cord, motor neurons of the brainstem, pyramidal cells of the cortex, and pyramidal tract of the spinal cord by unknown choice. The incidence is about: Because most patients die within 3 to 5 years of symptom onset, the prevalence of the disease is relatively close to the incidence.
MND** is not well understood, but it is generally believed that it is caused by the exposure of genetically susceptible individuals to adverse environments with age, i.e., a combination of genetic and environmental factors contribute to the development of MND.
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Zhou Guiyi mentioned: "Her undergraduate degree is in the Department of Architecture of Columbia University, in fact, it is a very big change from architecture to literature and art or directing.
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Hello, I went to the hospital for hospitalization**, and gave the ventilator oxygen infusion symptomatic **support**, and I will observe it.
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If patients with motor neuron disease have shortness of breath and difficulty breathing, they can use a ventilator to help the patient breathe, it is recommended that surgery and drugs can be used at ordinary times, and in the process, patients should pay more attention to rest, do not stay up late, and ensure sufficient sleep time.
The cause of the formation of motor neuron disease may be caused by motor neuron damage, the exact ** is not clear in medicine, motor neuron patients can be used with home ventilators, ** motor neuron disease can play an auxiliary role. Motor neuron disease is a disease of the nervous system, which will slowly affect the muscles of the patient's various systems, making the patient lose the ability to work and live, and may eventually affect the respiratory function.
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Motor neuron disease, as long as it is a ventilator produced by a regular manufacturer, it is recommended to buy a model under the guidance of a local doctor, there are not too many restricted brands, the price difference is large, and the basic functions can be purchased according to their own economic situation.
In recent years, the early use of non-invasive two-way positive pressure ventilation has formed a common standard in many countries, and it can actively assist the patient's inhalation to make the patient's inhalation comfortable and labor-saving.
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Spontaneous breathing can be caused by a variety of factors, but the most common is caused by damage to the respiratory center. For example, brain injury caused by cerebral vascular obstruction, stenosis or rupture, severe compression of brain tissue by intracranial hypertension or intracranial mass lesions, intracranial inflammation such as encephalitis and meningitis. There are also some patients who are unable to breathe spontaneously due to the loss of voluntary movement function of respiratory muscles, such as motor neuron disease, myasthenia gravis, etc.
Lesions of the respiratory system itself can also cause the occurrence of spontaneous breathing, such as open pneumothorax, severe pneumonia, etc.
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Not necessarily. Problems with any part of breathing can lead to the inability to breathe spontaneously, including abnormalities in the central drive of breathing, nerve conduction abnormalities, respiratory muscle dysfunction, and abnormal thoracic movements.
For example, traumatic brain injury, cerebral hemorrhage, inflammation, tumors and other damage to the respiratory center, neuromuscular diseases, such as myasthenia gravis, respiratory muscle dysfunction, and open pneumothorax and other thoracic diseases, can lead to impairment of respiratory function, so that it is impossible to breathe on its own.
In addition, some autonomic factors may also cause patients to feel dyspnea and unable to breathe on their own, which requires a comprehensive judgment based on the condition.
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Respiratory support is a method for respiratory diseases or injuries, mainly by training the strength and endurance of respiratory muscles, improving respiratory function and improving quality of life. Motor neurons are part of the nervous system that controls the movement of muscles, including those of the respiratory muscles. As a result, respiratory support** can have a positive effect on motor neurons.
Studies have shown that respiratory support** can increase the strength and endurance of respiratory muscles, improve respiratory function, and reduce symptoms such as breathlessness and fatigue. In addition, respiratory support** can also alter the metabolism and structure of respiratory muscles, promoting muscle regeneration and repair, thereby improving the function and health of respiratory muscles.
For motor neurons, respiratory support** can promote muscle movement and functional recovery by training the strength and endurance of respiratory muscles, strengthening neuromuscular connections, and improving motor neuron excitability and reaction speed.
In conclusion, respiratory support** can have a positive impact on motor neurons, improving the function and health of respiratory muscles and improving quality of life.
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MND can manifest as weakness and atrophy of the limbs, clumsiness and weakness of finger movements, muscle weakness and atrophy over the course of the disease, extending to the trunk and neck, and finally involving the facial and throat muscles. Patients may have bulbar paralysis, mostly in the late stage, the tongue muscles are first involved, manifested as tongue muscle atrophy, fasciculation, and tongue protrusion weakness, followed by pharyngeal, laryngeal, and masticatory muscle atrophy and weakness, resulting in the patient's slurred arthria, dysphagia, chewing weakness, and the orbicularis oculi muscle in the facial muscle is more obviously involved. There is often a pattern of disease progression in MND, usually from the upper extremity that is first affected, then to the contralateral upper extremity, to the ipsilateral lower extremity, to the contralateral lower extremity, and finally to the bulb involvement.
Motor neuron disease can be life-threatening, mostly within 3 to 5 years, death from respiratory muscle paralysis or lung infection, so motor neuron disease is more harmful. You can come to Beijing Renxuan Traditional Chinese Medicine to find Sheng Jinqiangfu**, and through one-to-one conditioning of Yiyuan Muscle Formula, the patient's symptoms can be improved.
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This is related to lung use, lung capacity is small, it is recommended to exercise moderately every day to enhance physical fitness and enhance lung capacity.
There will also be misdiagnosis of motor neuron disease, this situation needs to be examined in detail, generally the main feeling is unreliable, must be selected EMG evoked potentials, nerve conduction velocity is necessary, and the examination is carried out at the same time choose to go to a regular hospital for testing.
Motor neuron disease is a group of **unspecified choices** chronic progressive neurodegenerative diseases of bone marrow anterior horn cells, brainstem motor neurons, cortical pyramidal cells, and vertebral tracts. >>>More
The early stage of motor neuron disease is characterized by gradual muscle atrophy and weakness in one part of the patient's body, and many diseases have similar clinical manifestations in the early stage, and the age of onset of this disease is between 40 and 60 years old, which is also the stage of high incidence of cervical spondylosis. Many patients with cervical spondylosis can also have unilateral limb muscle atrophy and weakness in the early stage, so many patients mistakenly believe that it is cervical spondylosis, delaying the diagnosis. There is no difficulty in an advanced ALS person, and the diagnosis can be made by simply taking clinical data, but the difficulty in the examination of motor neuron disease is when it is atypical in the early stage, and it may be difficult to determine that it is an area of disease if there is no experience. >>>More
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Hope it helps. There is currently no reliable method for motor neuron disease, it is a refractory disease, and the survival rate after the disease is generally found to be about 5 years, but there are many types of motor neuron disease, and the survival rate is not the same, with an average of about 5 years. However, in recent years, there have been gradual reports in clinical practice: >>>More