Intentional Anticipatory Mourning, Caregiver and Bereavement Support Program for Terminally Ill Veterans, Their Families & Caregivers in the VA Contract Home Hospice Program

2013 ◽  
Vol 67 (1-2) ◽  
pp. 69-77 ◽  
Author(s):  
Donnamarie Flanagan-Kaminsky

As a response to the increasing numbers of Veterans utilizing the Veterans Affairs (VA) Contract Home Hospice Program, and with growing awareness of the increased stress at end-of-life, the social work leadership of the Louis Stokes Cleveland VA Medical Center implemented a unique approach to support Veterans and their families. The role of a grief/bereavement counselor was added to enhance the VA Contract Home Hospice Program, to assess the needs of the Veterans and family caregivers, and to create a program in response to these findings. A three-prong module evolved encompassing: Anticipatory Mourning Support for both the Veteran and caregiver/family; Caregiver Support; and Bereavement Support. The components of this module are described along with findings in each module.

1995 ◽  
Vol 23 (1) ◽  
pp. 44-49 ◽  
Author(s):  
Victor E. Jimenez-Lucho ◽  
Florence Fallon ◽  
Connie Caputo ◽  
Karol Ramsey

2020 ◽  
pp. 073346481990109
Author(s):  
Katarzyna A. Zebrak ◽  
Joanne R. Campione

Extant evidence on the effectiveness of caregiver programs in alleviating caregiver burden is mixed, underscoring the need for further investigations. This study evaluated the effect of the National Family Caregiver Support Program (NFCSP) educational services and respite care on caregiver burden. We used survey data from caregivers assigned to program ( n = 491) or comparison ( n = 417) group based on their reported use of NFCSP services. Adjusted difference-in-differences (DiD) analysis found an increase in mean burden scores for both groups from baseline to 6 or 12 months. Among program caregivers receiving ≥4 hr of NFCSP respite care per week ( n = 307) and matched comparisons ( n = 370), burden scores decreased slightly for program caregivers (−0.095 points), but increased for comparison caregivers (+0.145 points). The DiD (0.239 points) was not statistically significant. More research is needed to determine the minimum amount of respite care needed to positively impact caregiver burden.


1988 ◽  
Vol 69 (6) ◽  
pp. 376-379
Author(s):  
Sandra Napoleone

The author discusses inpatient care of persons with AIDS based on her experience at Davies Medical Center, San Francisco. Issues and concerns of patients and families are discussed, and the role of the social worker is described, especially with regard to first hospitalization.


2020 ◽  
Vol 63 (5) ◽  
pp. 381-393
Author(s):  
Joanna M. Gaitens ◽  
Benjamin K. Potter ◽  
Jean‐Claude G. D'Alleyrand ◽  
Archie L. Overmann ◽  
Michael Gochfeld ◽  
...  

2018 ◽  
Vol 39 (4) ◽  
pp. 347-356 ◽  
Author(s):  
Jane Strommen ◽  
Heather Fuller ◽  
Gregory F. Sanders ◽  
Dustin M. Elliott

The focus of this study was to identify challenges to family eldercare provision from the perspectives of both caregivers and community stakeholders. This qualitative study used data from 306 family caregivers and 116 stakeholders (aging, social, and health service professionals who work with older adults and their families) in North Dakota. Data sources included an American Association of Retired Persons-ND survey of 110 caregivers, a survey by the ND Family Caregiver Support Program (196 participants), and a Statewide Caregiving Stakeholder Survey (116 participants). Thematic analysis identified five themes: (a) financial burden of providing eldercare, (b) insufficient access to respite care, (c) difficulty finding and navigating available services and programs, (d) lack of knowledge and training on care provision, and (e) challenges related to environmental context of caregiving. Implications for working with family caregivers and developing policies for eldercare are discussed.


Sign in / Sign up

Export Citation Format

Share Document