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.