The 2003 Caregiver
Survey
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As part of the "Community Conversation on Caregiving," a survey of caregivers
was taken in the winter of 2003. The survey was distributed in various
forms, including the Ithaca Journal, the Senior Circle, the Office for
Aging website, and through direct mail. A total of 225 people completed
the Caregiver survey. Because this was not a scientific survey done
through random sampling, we cannot use the results to make generalizations
about all caregivers in Tompkins County; however, the results do provide
us with useful information about the characteristics and needs of those
caregivers who responded.
I. Who Are the Caregivers?
The majority of respondents
were adult children caring for their aging parents (61%), followed by those
caring for their spouse or partner (19%), friend or neighbor (10%) or other
relative (10%). Over three-quarters of the respondents (76%) stated
that they were the primary caregiver, that is the one most involved in
providing care for the person. Additionally, 20% of those who responded
were also caring for children under age 18.
Respondents were of
a wide variety of ages, with 73% under the age of 65. Over three-quarters
of the respondents were female (77%). Respondents had a wide variety
of income and educational levels. Sixty-three percent of respondents
were employed outside the home, with 46% employed full-time and 17% employed
part-time. Finally, most caregivers who responded lived either in
the same home as the care receiver or less than 20 minutes away.
II. For Whom Are the Caregivers
Providing Care?
The majority of respondents
are providing care for people age 70 or older (91%), and the majority of
care receivers are women (60%). Most care receivers are living in
their own home or apartment (71%). Respondents indicated that care
receivers had a number of medical conditions, the most common being arthritis,
heart problems and dementia, and 69% of people had more than one medical
condition. The majority of respondents (71%) indicated that the care
receiver has a health care proxy or living will.
III. The Tasks of Caregiving
Respondents provided
a wide variety of tasks for the care receivers, the most common being grocery
shopping, transportation, help with bills and regular phone contact.
The caregivers who responded provide these tasks from as little as few
times a month to several hours every day. An estimate of the total
number of hours of unpaid care provided by this sample of 225 people over
a one-month period is 14,726. Many respondents have provided care
for a number of years; the majority of which have provided help for between
0-4 years (42%), though a sizeable number have provided care for
over 10 years (18%).
IV. Stresses and Rewards
of Caregiving
Of those caregivers who
responded to the survey, 40% stated that others were providing them with
enough relief from caregiving tasks, 27% stated that they were not receiving
enough relief, and 33% stated that they had nobody else to help them.
When asked whether others were doing their fair share to help with caregiving,
50% stated "yes, as best as they can," while another 30% stated "no, they
are not," 11% stated they "have no other friends/family to help," and 9%
stated that tasks were divided evenly. Among the stressful aspects
of caregiving, respondents tended to cite "emotional stress" most often
(74%), followed by "not enough time for myself" (55%), and "sadness about
losses" (38%). Those who report that other family and friends are
not doing their fair share to help with caregiving cite these stressful
aspects of caregiving with greater frequency than overall respondents.
Caregivers also cited the effects of caregiving on employment, with 79%
of respondents who were employed stating that they had to go to work late,
leave work early, or take time off due to caregiving. Among the positive
aspects of caregiving, respondents tended to cite "helping family" most
often (68%), followed by "caring for others" (55%) and "being appreciated"
(44%).
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