Internet Stroke Center Home Stroke Information for Patients & Families
 

Patients & Families   Health Professionals   Clinical Trials   About   Home 


Search the ISC 
Search the Web
 About Stroke
What is a Stroke?
Types of Stroke
Warning Signs
Stroke Statistics
 Stroke Diagnosis
How a Stroke is Diagnosed
Lab Tests & Procedures
Blood Tests
 Stroke Treatment
Reducing Your Risk
Carotid Endarterectomy
Specific Medications
Clinical Trials & Drug Development
Links for Drug Information
 Living with Stroke
Recovering After a Stroke
Aphasia Information
Home Modification
Support Groups
Stroke Survivor Stories
Life After Stroke Video Series
 Caregivers
Introduction
Useful Links
 Stroke News
Recent Stroke News
Stroke News Archive
Sources for Stroke News
 En Español
¿Que es la embolia cerebral?
Otras Fuentes de Información
 Directories
Stroke Center Directory
Stroke Organizations
Stroke Links


Information for Caregivers

This information provided and prepared by Dorothy Edwards, Ph.D., Associate Professor of Occupational Therapy and Neurology at Washington University School of Medicine.


Caregiveramily caregivers and friends play a critical role in the recovery from stroke, particularly as lengths of stay in hospitals and rehabilitation settings continue to decrease. Stroke recovery continues for at least two years after stroke onset, so most of the support during this period comes from informal sources including friends and family members.

Providing care for a stroke patient can be an extremely rewarding experience. At the same time it can be very stressful and frustrating to be suddenly thrust into the position of caregiver with little or no warning. It is crucial therefore, to remember to cater to your own needs, in addition to those of the patient.

Also important to note is that stress tends to increase over time if the caregiver's needs are not met. Some of those needs may include the need for information (especially better understanding of the emotional and behavioral changes), the need for skills in the physical aspects of care, and the need for support in the “case management” aspects of care. In terms of emotional reactions, caregivers often feel one or more of the following: anxiety, guilt, depression, frustration, resentment, impatience, and fear. (Fear that a stroke may happen again, fear that the stroke survivor may be unable to accept the disabilities, fear that the survivor may require nursing home placement, fear that the caregiver may make mistakes, and fear that families and friends will abandon them.) Coping with these reactions is paramount to a healthier caregiver, and ultimately, to a healthier patient.

Stroke Family Caregiving for African-AmericansFor more information and tips on caring for stroke survivors, please visit Stroke Family Caregiving for African-Americans. Desiged specifically with African-American caregivers in mind, this site nontheless contains universal information for stroke family caregivers from all walks of life.

Related Video:

Caregiver Involvement in Post-Stroke Care

Useful Links


 

This site is a non-profit, educational service of Washington University School of MedicineInternet Stroke Center at Washington University:
TOP | HOME | ABOUT | PRIVACY POLICY | CONTACT

Copyright © 1997-2008 - Internet Stroke Center. All rights reserved.

The information contained in this web site is not a substitute for medical advice or treatment.
Consultation with your doctor or health care professional is recommended.