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Muscle atrophy occurs in MND, which can be chosen, oral vitamin E and vitamin B, or immunosuppressants can be selected for early progress** and prevention, and at the same time, you should choose, pay more attention to rest, and use neuroregenerative drugs**.
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Motor neuron disease is a relatively common disease, and many athletes will develop this disease, mainly due to long-term high-intensity exercise, which can lead to motor nerve injury, which can lead to the development of the disease. The onset of motor neuron disease is accompanied by significant symptoms of muscle atrophy and muscle weakness, which require adequate attention.
Motor neuron disease is no stranger to everyone, and many people in their lives are susceptible to this disease. The initial stages of MND can lead to certain physical injuries that may cause pain and numbness that most people do not pay enough attention to. When the disease progresses severely, it can lead to muscle wasting and muscle weakness.
So is muscle wasting a motor neuron disease? Next, we will introduce the symptoms and manifestations of motor neuron disease.
If you have muscle wasting, you may be suffering from MND, so you can't ignore it. If it is not controlled in time, it is likely to lead to limited movement in the body. Therefore, it is necessary to take an active ** at the onset of the disease.
Choose the appropriate method to do it** and be able to return to a healthy body as soon as possible. Motor neuron disease is extremely harmful to people's physical and mental health, and it is necessary to insist on early detection and early detection to get rid of the disease as soon as possible. After muscle wasting, it is advisable to eat more protein-rich foods.
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MND is a progressive disease, and it is necessary to control and delay the progression of the disease before considering how to improve the patient's symptoms.
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Neuromuscular atrophy is not a single disease, it is a general term for diseases that cause muscle atrophy due to neuropathy, including anterior horn lesions and peripheral neuropathy caused by various causes, **including **** and ****, anterior horn lesions of the spinal cord are most common in motor neuron disease and polio, there is currently no specific method for motor neuron disease, riluzole can be given orally, edaravone static point, and symptomatic support can be given at the same time**.
Poliomyelitis is currently prevented by oral vaccine, acupuncture is the mainstay, and nerve root compression or peripheral neuropathy caused by other causes can also cause muscle atrophy, such as the common Guillain-Barre syndrome, which is peripheral nerve damage caused by immune reasons, which can be given gamma globulin or plasma exchange, as well as autoimmune-mediated peripheral nerve damage due to other reasons, and can also be carried out with hormones and immunosuppressants. If it is due to compression by a tumor in the spinal cord or a herniated disc pressing on a nerve root, surgery may be given to relieve the compression. In addition, muscle atrophy can also be given acupuncture and ****.
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If the patient has motor neuron disease, these patients are prone to symptoms such as muscle atrophy and weakness. For these patients, a combination of multiple methods is often required, including acupuncture, symptomatic therapy, and exercise.
Such patients tend to be very long and costly. If it is not timely**, the patient may experience respiratory failure, dyspnea, etc. These patients require ventilators to assist ventilation if necessary, as well as endotracheal intubation.
If there is dysphagia and choking on water, a nasogastric tube diet is required to ensure the nutrition and energy of the patient's diet.
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Muscle atrophy occurs in MND, which can be chosen, oral vitamin E and vitamin B, or immunosuppressants can be selected for early progress** and prevention, and at the same time, you should choose, pay more attention to rest, and use neuroregenerative drugs**.
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You can try Chinese medicine, what are the symptoms now.
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Muscle atrophy occurs in MND, which can be chosen, oral vitamin E and vitamin B, or immunosuppressants can be selected for early progress** and prevention, and at the same time, you should choose, pay more attention to rest, and use neuroregenerative drugs**.
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Motor neuron is a relatively rare degenerative neurological disease, which is so rare that even hospital doctors don't know much about it, so it is often difficult to diagnose it. Continental Fighting.
Motor neuron is a disease characterized by progressive spinal muscular atrophy and amyotrophic lateral sclerosis, which is a progressive disease that progresses over time and has an increasing impact on life. When motor neurons are present, the more common early symptoms may be weakness and stiffness of finger movements, clumsiness of hand movements, and atrophy of hand muscles. Over time, it gradually expands to the forearms, pectoralis muscles, back, and even calves.
Weakness of the limbs, muscle stiffness, difficulty moving, difficulty breathing and swallowing, and in severe cases, spastic paraplegia of the lower limbs may occur.
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Motor neuron damage is the primary disease of this disease.
Vitamin E and B vitamins can be taken orally, along with coenzyme Q10, interferon, immunosuppressants, hepatocytes**, etc., which nourish nerves.
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In such a situation, you can carry out a massage to carry out **, coupled with appropriate protein supplementation, which can prevent our muscles from further atrophy, of course, we can use foreign objects to help our lower limbs to do a small amount of exercise.
Since the nature of MND is unclear, there is no specific approach. >>>More
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.
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
Motor neuron disease is a relatively common disease, and many athletes will develop this disease, mainly due to long-term high-intensity exercise, which can lead to motor nerve injury, which can lead to the development of the disease. The onset of motor neuron disease is accompanied by significant symptoms of muscle atrophy and muscle weakness, which require adequate attention. >>>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