Abstract
AbstractEpilepsy is a chronic brain disorder characterized by unpredictable seizures, significantly impacting emotional well-being and interpersonal relationships. Despite being a prevalent condition, pervasive myths and misconceptions persist, leading to stigma and societal discrimination. Disparities in epilepsy prevalence exist between affluent and impoverished nations, with higher rates observed in economically disadvantaged regions. In Pakistan, epilepsy affects over 2 million individuals, predominantly in rural areas, yet accurate diagnosis and treatment remain challenging due to limited access to specialized health care facilities and diagnostic tools like video electroencephalogram. Compounding this issue is the misdiagnosis of psychogenic nonepileptic seizures (PNES) as epilepsy, resulting in inappropriate treatments and increased health care costs. Addressing these challenges necessitates a multifaceted approach, including awareness campaigns to dispel myths, improving access to diagnostic tools and specialized care, enhancing health care provider training, and integrating epilepsy management into primary health systems. Collaboration between stakeholders, along with increased research efforts, is vital to ensure equitable access to diagnosis and treatment for epilepsy and PNES, irrespective of geographical location or socioeconomic status.
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