Page No: 297-307
Jaya Bharti
A.N.D.N.N.M.M. (C.SJ.M. University), Harsh Nagar, Kanpur
Pallavi Bhatnagar
University of Lucknow.
Caregivers of individuals with chronic mental illness experience a profound burden,
impacting their emotional, social, and physical well-being. The long-term stress of
caregiving can lead to burnout, social isolation, financial strain, and deteriorating mental
health. This study explores the subjective experiences of caregivers, highlighting their
challenges, coping mechanisms, and the impact on their quality of life. A qualitative
approach employing in-depth interviews with caregivers of individuals diagnosed with
chronic mental illness. A purposive sampling technique will be used to select participants
who have been primary caregivers for at least a year. Thematic analysis will be conducted
to extract key themes from their narratives. Preliminary findings suggest that caregivers
experience emotional distress (anxiety, guilt, helplessness), social withdrawal, financial
burden, and physical exhaustion. Many reported feelings of self-blame, frustration, and
depression. Additionally, their quality of life is shaped by factors such as access to
social support, coping strategies, and the availability of mental health resources. Despite
hardships, some caregivers demonstrate resilience, discovering personal growth, deeper
empathy, and a renewed sense of purpose through their caregiving journey. Addressing
the challenges faced by caregivers requires a holistic approach, incorporating mental
health interventions, social support networks, and policy reforms to ease their burden
and improve their well-being. The study underscores the need for psychological
counseling, community engagement, and financial aid to sustain caregivers in their
critical roles.