A 68-year-old woman presented with difficulty swallowing, speaking, and holding objects for 1-2 years. She was recently intubated for severe shortness of breath. Her symptoms were consistent with myasthenia gravis, which was confirmed by positive acetylcholine receptor antibodies and decremental response on repetitive nerve stimulation testing. She received pulse dose steroids, anticholinergics, and 4 cycles of plasmapheresis with improvement. Her vocal cords became mobile and she was discharged on steroids, azathioprine and anticholinergics.