Pachymeningitis as sequelae of systemic inflammatory diseases such as RA is rare, and recognition of its features are paramount. It can be an insidious, progressive cause of epilepsy and encephalopathy, and should be considered in older adults with new-onset epilepsy and no clear precipitating factors, even without a known history of systemic inflammatory disease. This condition is highly responsive to steroids and immunomodulatory therapy and should be suspected when drug-resistant epilepsy develops in the setting of clinical or lab-supported rheumatologic disease. Pachymeningitis can carry significant morbidity and mortality, therefore prompt treatment can greatly improve patient outcomes.