A 30-year-old female presented with one week of worsening ascending weakness, numbness, and pain in her lower extremities. She had lost 75 pounds in the past four months attributed to poor oral intake. On exam, she had no cognitive deficits and demonstrated severe weakness, areflexia, and decreased sensation to pain, vibration, and light touch in her lower extremities. Magnetic resonance imaging of the neuraxis was unremarkable. Cerebrospinal fluid basic studies were normal with no albuminocytologic dissociation seen. She was started on intravenous immunoglobulin for concern of GBS. Phosphatidyl ethanol 16:0/18:1 was 704 ng/mL. Thiamine was less than 2 nmol/L. Electromyography showed evidence of a sensorimotor radiculoneuropathy with no demyelinating findings aside from the left peroneal nerve. She was diagnosed with an acute axonal neuropathy secondary to thiamine deficiency. Thiamine supplementation was started and no signs of Wernicke’s encephalopathy were noted during her admission.