What you have to prove
Show one of: (A) disorganization of motor function in two extremities with extreme limitation despite prescribed treatment; OR (B) bulbar and neuromuscular dysfunction with difficulty with respiratory support, swallowing, or speaking.
Medical evidence SSA expects
Neurologist records, acetylcholine receptor antibody testing, EMG with repetitive stimulation, chest imaging (thymoma screen), and treatment history (pyridostigmine, immunosuppressants, IVIG, plasmapheresis).
Common misconceptions
Well-controlled MG on immunosuppression rarely qualifies. Refractory cases with repeated myasthenic crises requiring hospitalization typically meet the listing.