A 23-year-old woman with autoimmune thyroiditis came in with a four-month history of worsening asymmetric ptosis, diplopia, dysphonia, and severe dysphagia. The examination showed diplegia facialis, palatal droop, an absent gag reflex, and lingual weakness (2/5) with fasciculations, as well as proximal limb fatigability and respiratory insufficiency (Single Breath Count (SBC): 3). A brain MRI showed a non-enhancing tectal cystic lesion that looked like a low-grade glioma at first. However, the absence of long-tract signs and the fact that symptoms changed over time pointed to a neuromuscular junction disorder. The presence of anti-AChR antibodies confirmed the diagnosis of generalised Myasthenia Gravis. Even though the patient was stable at first, a respiratory infection caused a crisis that needed ICU admission and intravenous immunoglobulin. After aggressive immunotherapy and corticosteroids, she achieved significant recovery (SBC >20). During follow-up, she experienced intermittent diplopia, demonstrating a favourable response to immunomodulatory treatment and a gradual decrease in corticosteroid dosage.