“…The health of family members is affected by caring for children with thalassemia and reciprocally influences the illness of the affected children (Wright & Bell, 2009;Wright & Leahey, 2013). The mothers taking care of children with thalassemia experience emotional distress, fear of death, difficulties in managing personal feelings, and inadequate availability of supportive nursing services (Sapountzi-Krepia et al, 2006). Family caregivers also experience stress and anxiety, low self-esteem, and financial burdens (Wacharasin et al, 2006).…”