REFERENCES
- Biorn-Hansen V. Social and emotional aspects of aphasia. I Speech Hearing Disord. 1957;22:53–59.
- Malone RL. Expressed attitudes of families of aphasics. I Speech Hearing Disord. 1969;34: 146–151.
- Wells A. Family support systems: Their role in aphasia. Aphasiol. 1999;13:911–914.
- Chwat S, Chapey R, Gurland G, Pieras G. Environmental impact of aphasia: The child's perspective. Clin Aphasiol. 1980;10: 127–138.
- Denman A. Determining the needs of spous-es caring for aphasic partners. Disabil Rehabil. 1998;20:411–423.
- Herrmann M, Wallesch CW. Psychosocial changes and psychosocial adjustment with chronic and severe non-fluent aphasia. Aphasio/. 1989;3:513–526.
- Servaes P, Draper B, Conroy P, Bowring G. Informal carers of aphasic stroke patients: Stresses and interventions. Aphasiol. 1999;13:889–928.
- Williams SE. The impact of aphasia on mari-tal satisfaction. Arch Phys Med Rehabil. 1993;74:250–252.
- Zemva N. Aphasic patients and their families: Wishes and limits. Aphasiol. 1999;13: 219–224.
- Chwat 5, Gurland G. Comparative family perspectives on aphasia: Diagnostic, treat-ment, and counseling implications. Clin Aphasiol. 1981;11:212–225.
- McCue K. How to Help Children Through a Parent's Serious Illness. New York: St. Martin's Press; 1994.
- Rollin WJ. Family therapy and the aphasic adult. In: Eisenson J, ed. Adult Aphasia. Englewood Cliffs, NJ: Prentice Hall; 1984: 252–282.
- Labreche J. A most extraordinary week in the life of Mrs. Emma MacTavish. Communique. 1996;10:9–13.