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Family Education

Family Education




Family education for parents of children and adolescents




Family education or “psychoeducation” is the ongoing process of educating family members about a serious mental illness in order to improve their coping skills and their ability to help a relative affected by the illness.


When someone is diagnosed with a chronic illness, such as diabetes or heart disease, efforts are typically made by his or her doctor not only to educate the individual directly affected by the illness, but to educate and involve his/her family in treatment and care. Historically, this has not been the case with severe mental illnesses such as schizophrenia , major depression, bipolar disorder , or schizoaffective disorder.

Historically, most mental health professionals did not educate families about what to expect or how to care for their loved one. In fact, for much of the twentieth century it was believed that mental illness was caused by overly strict or overly permissive parenting styles, and families were unfairly blamed for causing these disorders. Mothers were labeled “schizophrenogenic” and even well-meaning clinicians tried to keep them and other family members at a distance. Bateson’s “double-bind” theory of the time suggested that contradictory messages and communications by parents were the root cause of the problem. Because of these ideas and the stigma associated with mental illness, families felt isolated and alone, with few resources to assist them. After diagnosis , the only recourse for most families was to go to public libraries to read and learn as much as they could on their own.

Over the last 20 years, however, advances in genetics, neuroscience, and imaging techniques have provided new evidence that severe mental illnesses are neurobiological in origin. With this scientific knowledge has come greater awareness and understanding that these are “no-fault” brain illnesses, and that neither families nor patients should be blamed. Rather, they both should receive the necessary information and support to help them better cope with these complex disorders.


In the United States and elsewhere, the large majority of individuals with severe mental illness live with their families and depend on them for housing, financial assistance, advocacy, and support. For this reason families require knowledge and skills to actively help their relative benefit from treatment, avoid relapse , and achieve recovery. Specifically, family caregivers require information about the illness and its symptoms, how to better communicate with their family member and professionals, the pros and cons of different treatment options, medications and their therapeutic uses and their adverse side effects, signs of relapse, availability of community services and supports, how to access benefits and entitlements, and how to handle crises or bizarre and troubling behaviors. Because living with an individual with a serious mental disorder can be very stressful, family education must also focus on teaching families about the importance of taking care of themselves.

The National Alliance for the Mentally Ill (NAMI) is an umbrella organization of more than 1,100 local support and advocacy groups in 50 states. The organization comprises families and individuals affected by serious mental illness who come together for family education, mutual support, and advocacy. Through conferences, support groups , and newsletters, family members have opportunities to educate one another and exchange experiences. NAMI has also made great inroads in teaching mental health professionals about the importance of educating family members and involving them in plans for the patient’s treatment and rehabilitation. On a more formal level, NAMI has sponsored Family to Family, a 12-week education course that has been attended by 50,000 family members in more than 42 states. Taught by family volunteers, this is the first peer program in family education in the United States.

Family education is slowly becoming an integral part of treatment, as the practice guidelines for professionals have begun to recommend its use. Families are also utilizing a new generation of books about mental illness—some written by professionals, and others written by, and for, family members. Families are also increasingly using the Internet to learn more about mental disorders.

Family education for parents of children and adolescents

Because major mental illnesses tend to occur in adolescence or early adulthood, most family interventions focus on parents of adult children. However, any parent of a younger child with an emotional or behavioral disturbance can testify to the extraordinary challenges involved in coordinating care. For this reason, more public and private agencies are beginning to provide training, information, education, and financial assistance to family members of children and adolescents with emotional disturbances. The results of research about family education interventions for parents of children with serious emotional disturbances are just beginning to emerge. Some research suggests that family participation improves service delivery and patient outcomes for this group. In a randomized controlled trial of the training of 200 parents who did or did not receive training, while there were no significant effects on child mental health status, those family members who were trained showed significant knowledge enhancement and increased effectiveness.


Recent research has provided evidence that family education and support leads to improved patient outcomes. For example, family psychoeducation provided by mental health professionals has such a compelling research base that it is considered a practice based on the findings of real-life studies of family education and support.

Another type of therapy discussed in the scientific literature has been used in China and India. The “family consultation” model uses individualized, private consultations between the family and a trained consultant to assist the family on an as-needed basis.



Torrey, E. Fuller. Surviving Schizophrenia: A Manual for Families, Consumers and Providers, 4th ed. New York: HarperCollins, 2001.


Archie, Suzanne, Jane Hamilton Wilson, Kevin Woodward, Heather Hobbs, Shelley Osborne, and Jean McNiven. “Psychotic Disorders Clinic and First-Episode Psychosis: A Program Evaluation.” Canadian Journal of Psychiatry 50.1 (Jan. 2005): 46–51.

Dunbar, Sandra B., Patricia C. Clark, Christi Deaton, Andrew L. Smith, Anindya K. De, and Marian C. O’Brien. “Family Education and Support Interventions in Heart Failure. A Pilot Study.” Nursing Research 54.3 (May-June 2005): 158–66.

Edelman, Perry, Daniel Kuhn, Bradley R. Fulton, and Gregory A. Kyrouac. “Information and Service Needs of Persons With Alzheimer’s Disease and Their Family Caregivers Living in Rural Communities.” American Journal of Alzheimer’s Disease and Other Dementias 21.4 (Aug.-Sept. 2006): 226–33.

Murray-Swank, Aaron B., Alicia Lucksted, Deborah R. Medoff, Ye Yang, Karen Wohlheiter, and Lisa B. Dixon. “Religiosity, Psychosocial Adjustment, and Subjective Burden of Persons Who Care for Those With Mental Illness.” Psychiatric Services 57.3 (Mar. 2006): 361–65.


National Alliance for the Mentally Ill (NAMI). Colonial Place Three, 2107 Wilson Blvd., Suite 300 Arlington, VA 22201-3042. Telephone: (800) 950-NAMI (6264) or (703) 524-7600. Web site: <>.

National Family Caregivers Association. 10400 Connecticut Avenue, #500, Kensington, MD 20895-3944. Telephone: (800) 896-3650 Fax: (301) 942-2302. Web site: <>.

National Mental Health Association (NMHA). 1021 Prince Street Alexandria, VA 22314-2971. Telephone: (800) 969-6642 or (703) 684-7722. Web site: <>.


National Institute of Mental Health. “Schizophrenia.” <>.

U.S. Department of Health and Human Services. Mental Health: A Report of the Surgeon General. Rockville, MD: U.S. Department of Health and Human Services, 1999. Available at: <>.

Irene S. Levine, PhD
Ruth A. Wienclaw, PhD

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