Mesothelioma and its treatment can significantly impact patients’ quality of life by causing physical symptoms, emotional distress, functional impairment, and financial burden. Pain, fatigue, dyspnea, and gastrointestinal disturbances can affect daily activities and overall well-being.

Additionally, the emotional toll of coping with a life-threatening illness, uncertainty about the future, and treatment-related side effects may contribute to anxiety, depression, and decreased quality of life. Supportive care services, symptom management strategies, and psychosocial interventions aim to address these challenges and improve patient’s quality of life throughout their journey with Mesothelioma.