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Liu Hong Mei
Neurology
About me
Graduated from the Medical Department of Xi'an Jiaotong University, postgraduate degree from Hebei Medical University, working in cardiology and neurology for 20 years.
Proficient in diseases
Specializes in treating neurological diseases such as encephalitis, meningitis, myelitis, cerebral hemorrhage, cerebral infarction, migraine, Guillain-Barré syndrome, Parkinson's syndrome, anxiety and depression, dizziness, headache, as well as cardiovascular diseases such as coronary heart disease, angina pectoris, aortic dissection, hypertension, diabetes, etc.
Voices
Is occipital neuralgia the same as trigeminal neuralgia?
Occipital neuralgia and trigeminal neuralgia are different; these are two distinct diseases with different onset times, affected areas, and pain characteristics. Occipital neuralgia generally occurs in the back of the head and is associated with cervical spondylosis, neck muscle tension, spasms, injury, trauma, and inflammation, typically triggering pain in the distribution area of the greater occipital nerve. Trigeminal neuralgia generally affects the distribution area of the trigeminal nerve, causing very intense pain, which may be like lightning or a burning sensation. It is typically triggered by washing the face, brushing teeth, or touching and can start and stop suddenly.
How do people with ALS eat if they can't swallow?
Patients with amyotrophic lateral sclerosis (ALS) who no longer have swallowing function can be given nasogastric feeding and intravenous hyperalimentation to maintain nutrition and electrolyte balance. For patients with respiratory difficulties or respiratory failure, oxygen supplementation can be administered. This can be combined with treatments such as acupuncture, physical therapy, massage, and heat application. It is important to prevent complications such as pulmonary infections, aspiration pneumonia, hypostatic pneumonia, lower extremity venous thrombosis, acute gastritis, gastric mucosal erosion, and gastrointestinal bleeding, which are common in later stages of ALS. With the loss of swallowing function and decreased immunity, these complications can occur more frequently and require proactive treatment to improve nutritional status.
How long does it take for someone with ALS to go from onset to paralysis?
Patients with amyotrophic lateral sclerosis generally progress from onset to paralysis within three to four years. The condition typically involves the progressive degeneration, degeneration, and necrosis of brain nerve cells. Severe and irreversible damage can occur in the brain, spinal cord, and peripheral nerves, also known as motor neuron disease. Motor neuron disease restricts our movement, speech, swallowing, breathing, and muscle activity, causing muscles to gradually atrophy and degenerate, leading to progressive weakness and paralysis. Even speaking, swallowing, and breathing functions degrade, potentially leading to respiratory failure and life-threatening situations, requiring proactive treatment.
How to exercise for swallowing difficulties in people with amyotrophic lateral sclerosis
Swallowing difficulties in amyotrophic lateral sclerosis primarily involve exercises for oral muscles. Improvement in the movement of oral muscles can alleviate symptoms of swallowing difficulties. Rehabilitation training for oral muscle disorders mainly includes enhancing the movements of the lips, tongue, and lower jaw. Individuals with amyotrophic lateral sclerosis who have brainstem damage and medullary damage may experience swallowing difficulties, water drinking issues, and cough choking, primarily due to sensory disturbances in the throat. By utilizing temperature and sensory stimulation, the sensation in the patient's throat can be restored, allowing them to perceive the temperature and taste of food, thus reducing aspiration. After brainstem damage, the cricopharyngeal muscle does not open, which can be improved through balloon dilation and medication to enhance swallowing function.
What should people with ALS do if they cannot eat?
People with amyotrophic lateral sclerosis who are unable to eat may try liquid and semi-liquid diets, using warm liquids, eating little by little. If they cannot consume a liquid diet, they may need to resort to nasogastric feeding. A gastric tube is used for feeding, through which high-nutrition, high-protein, and high-calorie diets can be provided to sustain and extend the life of those with the condition. Avoid overeating and engage in appropriate exercise, paying attention to the functions of the respiratory and digestive systems. If there is excessive saliva, a small amount of antihistamine medication can be administered. If there is an excess of phlegm, nebulized inhalation and expectorant medications might be provided. If feeding through a gastric tube is also limited, intravenous nutritional support can be given.
Is amyotrophic lateral sclerosis (ALS) contagious?
Amyotrophic lateral sclerosis (ALS), commonly known as Lou Gehrig's disease, is not contagious. It is a genetic disease associated with autosomal dominant inheritance and is not considered an infectious disease. The exact cause of ALS is still unclear. Commonly identified mechanisms include genetic factors, inflammatory agents, excitotoxic effects from amino acids, infections, autoimmune factors, exposure to toxins, and heavy metal poisoning from metals like lead, mercury, and aluminum. Other contributing factors may include a deficiency in nerve growth factors, mitochondrial dysfunction, and apoptosis. These factors may likely be involved in the development of ALS symptoms, but the disease is not communicable.