What are the symptoms of MND?

The clinical manifestations of motor neuron disease are mainly lack of strength and muscle atrophy, the muscle atrophy is mainly interosseous muscles and thenar muscles, no strength is first manifested as the inability to lift heavy objects, at this time the condition is mild, will not affect daily life, when the disease further develops, there may be dysphagia, hoarseness, etc., in severe cases, there will be paralysis of respiratory muscles, and then severe respiratory suffering and life-threatening, but the body's sensory nerves are not damaged, all sensations are normal.

Motor neuron is also known as ALS, as the name of the disease suggests, patients will gradually appear as if they are "frozen", and the patient will gradually develop from limb weakness to muscle atrophy; The limbs gradually develop from the hands and feet, and eventually to the torso. Patients may experience dyspnea, dysphagia, and most eventually die of paralysis of the respiratory muscles. At present, Western medicine does not have a good method for motor neurons, but there is no way for motor neurons, and choosing the right professional method as soon as possible plays a vital role in motor neurons.

Motor neuron is an incurable disease, and the most important thing is to treat the symptoms**, so that it will slowly recover.

MIN TCM belongs to the category of dysentery, and the soup of MIN Jin Quan Yuan can be used as a reference. In terms of diet, most of them are high in protein.

Manifested as limb weakness, tightness, and inactivity. Symptoms begin in both lower extremities and then spread to both upper extremities, with severe symptoms in the lower extremities. Weak limb strength, increased muscle tone, difficulty gait, spasmodic scissor gait, hyperreflexia, positive pathological reflexes.

If the lesion involves both cortical brainstems, symptoms of pseudobulbar palsy appear, manifesting as clear speech, dysphagia, and mandibular hyperreflexia.

The early symptoms of motor neurons are not obvious, so many patients have difficulty wiping them in the early stage. The general course of the disease progresses slowly, but some types may progress more rapidly. Depending on the site of injury, the clinical manifestations are a different combination of muscle weakness, amyotrophy, and dysphagia.

Through the regulation of the human liver, kidney, spleen and stomach, the five elements of Jiyuan decoction are treated with the movement of five substances: wood, fire, earth, metal and water, and the five elements complement each other.

The most common first symptom of amyotrophic lateral sclerosis is clumsiness and weakness in one or both fingers, followed by atrophy of the small finger muscles that progresses to the forearm, upper arm, and shoulder muscles. As the disease progresses, muscle weakness and atrophy extend to the trunk and neck, and eventually to the facial and laryngeal muscles. In a few cases, muscle atrophy and weakness begin in the lower extremities or trunk.

Fasciculations are often evident in the affected area. The common first symptom of progressive amyotrophy is atrophy and weakness of the small muscles in one or both hands, which gradually affects the muscles of the forearm, upper arm, and shoulder. Affected muscles are markedly atrophied, muscle tone is reduced, and muscle tremors may be seen.

Progressive bulbar palsy is characterized by progressive slurred articulation, dysphagia, choking on water, and weakness in chewing. The tongue muscles are obviously atrophied, and there are fasciculations, and the lip muscles and throat muscles are atrophied. This type of disease progresses rapidly, and most of them die within 1 to 2 years due to respiratory muscle paralysis or lung infection.

The common first symptom of primary lateral sclerosis is symmetrical stiffness and weakness in both lower extremities, with a scissor gait in walking. Progresses slowly and gradually affects both upper extremities. There is usually no muscle atrophy and fasciculations, and no sensory deficits.

This type progresses slowly and can survive for a long time. Other symptoms: A small percentage of patients with motor neuron disease have manifestations outside the motor system, such as dementia, paresthesias, and urinary and urinary dysfunction, and a small number of patients have extraocular muscle movement disorders.

Progressive muscle atrophy and analopathy paralysis are typical symptoms, and patients may have difficulty walking and daily activities, weakness of the lower limbs, slurred speech, and difficulty swallowing. It can be done through drugs** and traditional Chinese medicine**.

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Symptoms of motor neuron disease mainly include muscle weakness, muscle atrophy, bulbar palsy, pyramidal tract sign, etc. Muscle weakness and muscle atrophy: patients initially present with small muscle atrophy and weakness in one or both hands, which gradually develops to involve the forearm, upper arm and shoulder blades, and some patients begin to have muscle atrophy and weakness in the lower limbs, and eventually develop into generalized muscle atrophy and weakness after several or more years, and cannot take care of themselves.

What are the symptoms of MND?

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The symptoms of the disease mainly include muscle weakness, muscle atrophy, bulbar paralysis, pyramidal tract signs, etc. Muscle weakness and muscle atrophy: patients initially present with small muscle atrophy and weakness in one or both hands, which gradually develops to involve the forearm, upper arm and shoulder blades, and some patients begin to have muscle atrophy and weakness in the lower limbs, and eventually develop into generalized muscle atrophy and weakness after several years or more than ten years, and cannot take care of themselves.

Hello dear, motor neurons are mainly some structures of the nervous system related to movement, anatomically it will be divided into upper motor nerve key meridian element and lower motor neuron, upper motor neuron refers to the brain center, some nerve cells on the cerebral cortex are called large pyramidal cells, and these cells will send out some nerve axons, these axons synapses form a nerve central nervous system, descending to the anterior horn cells of the spinal cord, to the part above the anterior horn cells of the spinal cord, all of which are called middle and upper motor neurons.

The early manifestations of MND are often atypical, taking the most common amyotrophic lateral sclerosis as an example, the early clinical manifestations are diverse, and there is a lack of specific biological diagnostic indicators. Most patients have a single upper limb onset, and the first manifestation is inflexibility and weakness of finger movement, and patients have difficulty extending the wrist, thenar muscle and vermiformis muscle. The small muscles of the hand are atrophied and gradually develop upward, the muscles of the forearm, upper arm and shoulder girdle are affected, and the extensor weakness is more obvious than the flexor weakness, and at the same time or subsequently, spasmodic paralysis of the lower limbs appears, and the physical muscle tone increases, tendon hyperreflexia, and positive pathological signs, and a few cases start from the lower limbs and gradually involve both upper limbs.

Muscle fibrillation is also a common symptom, which can occur in the muscles, tongue, and limb muscles innervated by the medulla, and a few can also be the first symptoms, and some patients may have symptoms such as dysphagia and tongue muscle atrophy. Patients may have subjective paresthesias, such as numbness, pain, etc. However, even in the advanced stages of the disease, there is no objective sensory impairment, and the paresthesias in some patients may be related to peripheral nerve entrapment.

For patients who are in the early stage of the onset response, clinically atypical, or have an unclear progression course, they should be followed up regularly and generally every 3 months to re-evaluate and diagnose.

Motor neuron disease has a slow onset and can be subacute. Symptoms depend on the early site of the lesion. The earliest symptoms are mostly seen in the hand, the patient feels weakness, stiffness, clumsiness of finger movements, and the muscles of the hand gradually atrophy, and fasciculations can be seen.

If the early lesion is located in the motor nerve nucleus of the medulla oblongata, dysphonia and swallowing, paralysis and atrophy of the tongue muscles, and fasciculations can be seen on the tongue surface.

At present, the cause of this disease is not clear, and it is generally manifested as weakness of the limbs and inability to move normally, generally degenerative diseases such as the forefoot cells of the spinal cord and brainstem motor neurons. Skeletal muscle can accumulate throughout the body. Be positive**.

It is necessary to go to the neurology department of the hospital to improve the relevant examinations and make a clear diagnosis, so as to treat the symptoms**. Dietary conditioning focuses on increasing nutrition to enhance physical fitness; Avoid tobacco and alcohol. Avoid colds.

Typical symptoms: upper and lower motor nervous system involvement is the main manifestation. Common symptoms:

Muscle weakness, muscle atrophy, and fasciculations are manifestations of lower motor nervous system involvement; Hypertonia, hyperreflexia, and positive pathological signs are the main manifestations of upper motor nervous system involvement. Other symptoms: the presenting symptom can be a variety of manifestations depending on the patient.

Most patients have asymmetrical local limb weakness, such as stiff walking, procrastination, easy falling, and inflexible finger movement. Bulbar symptoms such as dysphagia and dysarthria. A small number of patients present with respiratory symptoms.

The symptoms of motor neurons are: 1. Movement disorders: including muscle atrophy, muscle beating and trembling, stiffness of hands and feet, inconvenience in walking, etc.;

2. Speech disorders: including dysarthria, tongue muscle atrophy, tongue muscle tremor, slurred speech, easy to choke, bulbar paralysis, etc.;

3. Pyramidal tract signs: including tendon hyperreflexia, positive pathological signs, increased muscle tone, etc.;

4. Normal autonomic nervous function: no sensory impairment, normal urine and bowel movements, and normal sexual function.

Motor neuron disease is a neurodegenerative disease that primarily affects the motor system and not the sensory system. Motor neuron disease (MND) also invades upper and lower motor neurons, and often begins with weakness of the small muscles in one hand, accompanied by atrophy, and gradually progresses to other limbs, eventually affecting the respiratory and swallowing muscles, causing dyspnea and swallowing.

Motor neuron disease often progressively worsens, the course of the disease is about 3-5 years, you can come to Beijing Renxuan TCM to find Sheng Jinqiangfu**, through Yiyuan Muscle Formula one-to-one conditioning, can improve the patient's symptoms.

Motor neuron disease is a disease that has a great impact on the motor function of the human body, and can cause paralysis in severe cases. Therefore, it is very important for patients to choose the best method at the best time, a good method can not only make the body less harmed, but also greatly reduce the cost, so patients must not delay the disease, timely treatment is the last word.