A previously healthy 24-year-old Native American woman presented to an outside facility in northern Arizona with a three-week history of generalized weakness and paresthesia, preceded by two weeks of nausea, vomiting, and severe constipation. Suspected Guillain-Barré Syndrome based on her weakness and areflexia led to a five-day course of IVIG without symptomatic improvement. She was then transferred to our facility for higher level of care. Behavioral changes including social withdrawal, visual hallucinations, and uncharacteristic outbursts were additional symptoms upon her arrival. On examination, she had persistent tachycardia, significant abdominal distension, hypophonia, generalized muscle weakness, hypotonia, absent deep tendon reflexes, and reduced sensation in all modalities. Her CSF analysis revealed a mildly elevated protein level of 62mg/dl with normal WBC and glucose. MRI brain and total spine were unremarkable. With concerns for autoimmune encephalitis with polyneuropathy, she received a three-day course of methylprednisolone, though without improvement. Extensive lab tests for autoimmune, paraneoplastic, toxic/metabolic, and infectious causes were negative. The diagnosis remained elusive until nursing staff discovered that her mother was regularly administering peyote as part of a religious practice.