How is MND treated?

Motor neuron disease is a very rare disease in neurology, how can it be done now? Because it is a very slow degenerative disease, it is more difficult to degenerate. At present, the only drug we use is Lirutai, but this drug is very expensive, and the domestic drug may cost about 70,000 or 80,000 a year.

There are neuroprotective drugs, such as edaravone, which can be used, but in general this drug may only delay the progression of the disease, and it is difficult to achieve **.

Motor neurons can be used to delay the progression of the disease with traditional Chinese medicine.

1.Vitamin E and vitamin B are taken orally.

2.Coenzyme intramuscular injection, citicoline intramuscular injection, etc.**, can be used intermittently.

3.For muscle spasms, diazepam, orally, chlorphenamine butyric acid, can be taken in divided doses.

4.Some drugs such as thyrotropin-releasing hormone, interferon, lecithin, testosterone, cysteine, immunosuppressants, and plasma exchange can be tried for this disease, but their efficacy is difficult to assess.

5.In recent years, with the development of stem cell technology, stem cells have become one of the means of the disease, which can alleviate and improve the disease.

6.Massage of the affected limb, passive movement.

From the perspective of modern medicine, there is no special method for amyotrophic lateral sclerosis, most of the interventions are aimed at the treatment and management of symptoms, and the multidisciplinary joint model can provide patients with better ** and nursing effects. In the United States, the drugs approved by the US Food and Drug Administration for amyotrophic lateral sclerosis are riluzole and edaravone. According to the survey, most patients will choose to use the above two drugs to delay the progression of the disease after being suspected or diagnosed.

In addition, antioxidant and neurotrophic drugs such as coenzyme Q10, vitamin E, complex B vitamins, methylcobalamin, and nerve growth factor are also common clinical drugs, but no obvious disease prognosis improvement effect has been observed.

For patients with advanced stages of severely impaired function, mechanical ventilation and percutaneous gastrostomy remain necessary supports**. In addition, stem cells** and genetic interventions, as well as a variety of new early medicines, are still in the research stage. Patients in China can also choose to use traditional Chinese medicine to improve symptoms and delay the progression of the disease.

Adhere to the diagnosis and treatment of diseases with traditional Chinese medicine, and under the guidance of the theory of putting forward the strange meridians, we have created a complete set of first-class systems based on the characteristics of traditional Chinese medicine. Emphasizing the unique theoretical system of treating the Qi Jing from the Qi Jing, combining the five visceral syndromes and the three focal points, using the best methods of regulating and supplementing the Qi Jing, Fu Yuan and raising the muscles, combined with the molecular biotechnology of modern medicine and the latest research and development results, a series of preparations for motor neuron disease have been successfully developed.

For example, ** Ginseng Qi Strong Capsule for muscle atrophy; **Memory loss, limb atrophy, and body sleepiness; **Mental depression, muscle beating, nervous and anxious jujube even calming the nerves; **Muscle stiffness, muscle tremor symptoms of turtle peony flat tremor; **Qilong, which is not easy to cough up with unclear arthria, chest tightness and shortness of breath, low tone, timidity, phlegm and is not easy to cough up; **Weakness in chewing, difficulty swallowing, choking on food, and ginseng and ochre with puffing cheeks and leaking air, etc. Through a large number of clinical practices, innovative development methods, including directed muscle growth method, sacral duct, dysphagia as a whole, traditional Chinese medicine external plaster rubbing, traditional Chinese medicine collapsing, traditional Chinese medicine fumigation, wax therapy and other series of methods. It can play a good role in delaying the development of the disease, improving the quality of life of patients, reducing the pain of patients, and prolonging life.

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, so that the patient has unclear articulation, difficulty in swallowing, difficulty in chewing, and orbicularis oculi muscle involvement is more obvious in the facial muscle. 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**, Cong Mo can improve the patient's symptoms through one-to-one conditioning of Yiyuan Muscle Formula.

Wary! **Motor Neuron Disease, avoid falling into the following pitfalls:

Myth 1: It is considered to be an incurable disease: for a period of time, there is no obvious effect, there is often no hope of the disease, the disease continues to develop or acres, delays the development of the disease, and aggravates the development of the disease

Missale contains area 2: emergency medical treatment phenomenon: after discovering the condition, they are in a hurry to seek medical treatment, and often take some inappropriate methods, such as taking some western medicine to control it. Western medicine is so large that it can cause inflammation and stomach bleeding.

Myth 3: Superstitious home remedies or secret recipes: hearsay, trying to spend a little money or no money to treat diseases, this is the most undesirable, and there is no scientific basis for group laughter.

The treatment of motor neuron disease is as follows:

1. Drugs**: anti-excitant amino acid toxic drugs can be used to delay the development of early hunger diseases, and muscle relaxants, antioxidants, etc. can reduce patients' joint contractures, joint stiffness, drooling and other symptoms;

2. Oxygen therapy: For patients with respiratory weakness, oxygen therapy can be carried out through a simple home ventilator to reduce the symptoms of dyspnea or respiratory failure;

3. Surgery**: If the patient has swallowing dysfunction, the gastric tube can be indwelled in the short term, and the gastric comic fistula can be performed in the long term;

4. Psychology**: Psychological assessment and psychological counseling can help patients understand and face diseases.

The specific medication should be combined with clinical practice, and the doctor's face-to-face guidance shall prevail.

Hello dear, it is a pleasure to serve you.

Find out how to find out how to use motor neuron disease.

Motor neuron disease mainly relies on drugs ** and symptomatic **.

Drugs**. 1.Riluzole: taken continuously for 12 to 18 months, it can delay disease progression and prolong the survival of patients with progressive bulbar palsy.

2.Other medications: Your doctor may also choose prednisone, cyclophosphamide, neurotrophic factor, etc.

Symptomatic**. 1.Complications and accompanying symptoms such as swallowing, breathing, articulation, spasticity, pain, nutritional disorders**.

2.People with dysphagia are intubated and fed through a tube.

3.People with respiratory failure cut their trachea if necessary and use a ventilator to assist in breathing.

I wish you good health and happiness every day

Motor neuron disease can generally be relieved by medication, ventilators, etc. Motor neuron disease generally presents with hyperreflexia and positive pathological reflexes. **The drug for MND is called riluzole, which usually slows the course of the disease for a few months, but it is not very effective.

If the patient has respiratory muscle involvement and dyspnea, it is necessary to use a ventilator to assist breathing as soon as possible, which is the main means of prolonging the patient's life.

1.Drugs**, patients can use antioxidant drugs and muscle release drugs to relieve symptoms such as joint stiffness and contractures, and can be combined with the use of anti-excitable amino acid toxic drugs, which is conducive to delaying the progression of the disease and improving clinical symptoms.

2.Oxygen**, most patients with MND will experience respiratory weakness in the later stages of development, and oxygen therapy can be done with a simple ventilator at home to help relieve the symptoms of dyspnea.

3.Surgery**, if the patient has significant swallowing dysfunction, a gastric tube can be used for a short period of time, and gastrostomy surgery can be performed if necessary.

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.

At present, there are many patients with motor neuron in the world, but so far there is no specific solution. Motor neuron disease, also known as ALS syndrome, once the disease is obtained, the patient only damages the motor function, not the sensory function, the autonomic nervous system, and the patient's intelligence or emotion.

At present, there is no specific method, and most clinical doctors, ** to ** mainly, recommend that patients increase ** training. On the whole, there are more studies in this area, but in the past two years, the FDA in the United States recommended the best method for the sports god to shout brother Jingyuan disease, which is to use a large dose of drugs to scavenge free radicals and apply them intermittently for a long time. For example, edaravone seems to be effective for some patients after application, but the effect is not very good in clinical observation.

In short, there is no good way to do it, and it is hoped that through further research, a better solution will be provided in the future.

Motor nerve hypertonic disease itself is an unknown ** progressive neurodegenerative disease, the appearance of this disease caused by many complications will lead to movement disorders, speech disorders are more easily excited, and may even appear perceptual impairment, so what are the initial symptoms? Let's take a look at the symptoms of motor neuron disease.

1. Symptoms of motor neuron disease.

Patients will have weakness in the hands and feet at the beginning, atrophy is a relatively common symptom, at the beginning may appear on one side, then on the opposite side, and with the gradual development of the course of the disease, so there will be a mixed damage hole damage symptoms, in the late stage, the muscles of the whole body may appear atrophy, resulting in the patient can not raise his head normally, accompanied by dyspnea, can only be bedridden for a long time, Most of these diseases are most likely to occur between the ages of 40 and 60, with a 50 out of 10 chance of inheritance.

2. The dangers of motor neuron disease.

1. Movement disorders.

In the initial stage, the patient will have clumsy movements of the hands and feet, the lower limbs are also very prone to tripping, and there may also be tonic muscle spasm, which is a more common movement disorder, including cerebellar ataxia or spastic paralysis, so the complications are more serious and must be accepted as soon as possible**.

2. Speech disorder.

Most of them may be due to the patient's pseudobulbar palsy or cerebellar lesions, so there will be a phenomenon that the voice is not light or heavy, and even the vocal cords will be paralyzed, resulting in the patient having no way to talk normally.

3. Emotions are easily agitated.

This type of patients often have the phenomenon of emotional agitation, and the understanding will gradually be lacking, accompanied by obvious memory loss, muscle weakness, especially the distal muscles of the upper and lower limbs will also have obvious muscle weakness, and it is easy to lose muscle volume.

4. Sensory impairment.

Sensory impairment is often caused by spinal cord lesions, the most common symptoms of patients are numbness, accompanied by the effect of acupuncture, and sometimes cold or burning sensations, all of which are caused by diseases.

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 finally develop 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 any good methods for motor neurons, but motor neurons are not scum, and choosing the right professional method as soon as possible plays a vital role in the development of motor neurons.

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

The ** of motor neuron disease includes **, symptomatic ** and various non-pharmacos**. Motor neuron disease is a heterogeneous group of diseases, and the pathogens may be diverse and affect each other, so it must be a combination of multiple methods, and it is unrealistic to expect to completely block the progression of the disease with a single drug or a single species. So far, there is still a lack of drugs that can effectively reverse or control the development of the disease, the current development direction includes anti-excitatory amino acid toxicity, neurotrophic factors, antioxidant and free radical scavenging, anti-apoptosis, gene ** and neural stem cell transplantation, riluzole has the effect of inhibiting glutamate release, which may delay the course of the disease and prolong the survival of patients with bulbar paralysis, but there is no significant improvement in the muscle strength and quality of life of patients.