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Topics in Stroke Rehabilitation Volume 7, 2001 - Issue 4: Orthotic Management in Stroke
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Medical Grand Rounds

Addressing the Needs of Adolescent Children When a Parent Becomes Aphasic: One Family’s Experiences

Ann Harlowresides in Carmel, Indiana
&
Laura L. MurrayDepartment of Speech and Hearing Sciences, Indiana University, Bloomington, Indiana
Pages 46-51 | Published online: 23 Feb 2015

REFERENCES

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  • 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.
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  • 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.
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  • 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.

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