Can people with myasthenia gravis eat mangoes?

Written by Liu Hong Mei
Neurology
Updated on October 31, 2024
00:00
00:00

Patients with myasthenia gravis can eat mangoes and should consume more fresh vegetables and fruits. Mangoes are rich in flesh and fiber, and they taste sweet. They can help reduce cholesterol, quench thirst, promote blood circulation, improve circulation, and provide vitamins. Therefore, if patients with myasthenia gravis are not allergic to mangoes, they can include them in their diet. Mangoes contain a high amount of vitamins and are very nutritious. They also help facilitate bowel movements. Patients with myasthenia gravis should maintain a light diet, consuming foods that are high in protein, nutrition, and vitamins, and avoid spicy, stimulating, and exciting foods.

Other Voices

doctor image
home-news-image
Written by Zhang Hui
Neurology
49sec home-news-image

What should not be eaten in the case of myasthenia gravis?

Myasthenia gravis is an autoimmune disease of the nervous system, primarily due to dysfunction at the neuromuscular junction, leading to skeletal muscle fatigue. Symptoms include drooping eyelids, double vision, overall weakness, and even swallowing difficulties. Foods that should be avoided in myasthenia gravis mainly include certain medications, such as aminoglycoside antibiotics, which should not be taken orally by patients, as well as fluoroquinolone antibiotics. These antibiotics can exacerbate neuromuscular transmission disorders, potentially worsening the disease. Additionally, benzodiazepines, barbiturates, and some anti-arrhythmic drugs can also reduce muscle membrane excitability and should be avoided.

doctor image
home-news-image
Written by Zhang Hui
Neurology
47sec home-news-image

Myasthenia gravis should see which department?

Myasthenia gravis is a common disease in neurology, so when visiting the hospital, it is definitely necessary to see a neurologist. Neurologists have certain experience in diagnosing and treating this disease. This disease is classified as a neuromuscular junction disorder, mainly caused by the production of antibodies against acetylcholine receptors in the body. This leads to the nerve impulses not being effectively transmitted to the muscles, resulting in clinical manifestations. Patients' symptoms include improvement in the morning and worsening in the evening, fluctuating symptoms, and may present with drooping eyelids, double vision, general weakness, and some patients may also experience difficulty swallowing and speech disorders.

doctor image
home-news-image
Written by Shi De Quan
Neurology
36sec home-news-image

How to treat myasthenia gravis with pneumonia?

The treatment of pneumonia in patients with myasthenia gravis is the same as that for typical pneumonia, using corresponding antibiotics for bacterial, viral, or other microbial infections. However, if a patient with myasthenia gravis has a concomitant lung infection, aminoglycoside antibiotics, which can exacerbate conditions affecting neuromuscular junctions, i.e., worsen myasthenia gravis, should not be used. Sedative drugs are also contraindicated, as well as any drugs that might intensify muscle weakness.

doctor image
home-news-image
Written by Zhang Hui
Neurology
40sec home-news-image

Causes of myasthenia gravis

Myasthenia gravis is a type of neurological autoimmune disease. The cause and mechanism of this disease are primarily due to disorders in the immune function of the body. Antibodies are produced in the body which attack the acetylcholine receptors at the neuromuscular junction, leading to the failure of nerve impulses being transmitted to the muscles. This results in the clinical symptoms observed. Many patients may have thymic abnormalities, such as thymomas. Treatment of this disease involves the use of cholinesterase inhibitors and suppression of these abnormal immune responses, typically requiring the use of corticosteroids.

doctor image
home-news-image
Written by Tang Bo
Neurology
1min 2sec home-news-image

Does myasthenia gravis require hospitalization?

Myasthenia gravis in its early stages requires hospital treatment. It is an autoimmune disease characterized by a post-synaptic membrane failure at the neuromuscular junction due to decreased acetylcholine. It generally manifests as skeletal muscle weakness, with symptoms often being lighter in the morning and more severe by evening, and includes easy fatigability. In such cases, even without a definitive diagnosis, hospitalization is essential for accurate diagnosis and treatment, which may involve steroids or pyridostigmine. Treatment must be directed by a doctor. Once the condition stabilizes, the patient can be discharged and continue with oral medication. However, if a myasthenic crisis or other critical conditions occur, immediate hospitalization is necessary to maintain vital signs, as these situations can be life-threatening.