55-year-old Male with history of Hypertension presented with acute change in voice and paresthesia. On the third day, patient started having double vision and gait instability. On exam, patient had bilateral ptosis, dysarthria, hyper nasal speech, bilateral glove and stocking type paresthesia with no loss of strength, diffuse areflexia and ataxia. MRI of spine did not reveal any peripheral nerve root enhancement. CSF studies showed normal cell count and protein levels. EMG/NCS revealed bilateral mild to moderate ulnar and median neuropathy, normal on Lower extremities. He was also monitored for respiratory compromise. Labs for autoimmune antibodies were sent including Myasthenia antibodies, GM1 and GD1B which were all negative, However GQ1b antibody returned positive with a titer of 1:6400