TOPIC To describe the lived experiences of male caregivers of severely ment
ally ill relatives and their perceptions of this nontraditional role.
METHODS. A qualitative study of informal interviews with purposively select
ed male caregivers (N = 10), using an informal interview guide that address
ed psychosocial, physical, financial, and crisis-management categories.
FINDINGS. The data yielded three themes of caregiving: expressions of burde
n, duration and depth of commitment, and role affirmation.
CONCLUSIONS. The results can help health professionals develop needed educa
tion and support services for men in this emerging role and contribute to f
amily health in the community.