Caring for the Caregiver: Dementia

Similar documents
BEHAVIORAL HEALTH IS KEY TO LONG-TERM CARE REFORM

Statistical Portrait of Caregivers in the US Part III: Caregivers Physical and Emotional Health; Use of Support Services and Technology

Group-Based Interventions for Caregivers of Individuals with Chronic Health Conditions. Kelly Valdivia, BA and Stacy A.

Who Cares? Public Policy on Support for Alzheimer s Disease Caregivers. Emma Quinn. Writing 50. Gina Vallis

The Role of Religious Coping in Alzheimer s Disease Caregiving

How Managed Long-Term Services and Supports Can Help Family Caregivers

Policy Clarification for Caregiver Services and Respite Options for Families of Older Adults

Caregiving: Health Effects, Treatments, and Future Directions

End-of-Life Care and the Effects of Bereavement on Family Caregivers of Persons with Dementia

CAREGIVING COSTS. Declining Health in the Alzheimer s Caregiver as Dementia Increases in the Care Recipient

Alan B. Stevens, PhD Reference List

REACH II. Procedures. REACH II Intervention. REACH OUT II: Revision, Maintenance, and Sustainability. Project Funded by RCI/Johnson and Johnson

Supporting Caregivers -

Enhancing Quality of Life of Families Who Use Adult Day Services: Short- and Long-Term Effects of the Adult Day Services Plus Program

Caregiver Well-Being: Assessment, Interventions & Community Resources. Inter-Professional Panel

Consultation with RCI in Georgia

Flexible respite for carers of people living with dementia

Evidenced-Informed Training Intervention For Puerto Rican Caregivers of Persons with ADRDP

Family caregiving and emotional strain: associations with quality of life in a large national sample of middle-aged and older adults

INTRODUCTION. In our aging society, the challenges of family care are an increasing

State Strategies to Support Family Caregiving Susan C. Reinhard, RN, PhD

DEPARTMENT OF ELDER AFFAIRS PROGRAMS AND SERVICES HANDBOOK. Chapter 6. Administration of the Alzheimer s Disease Initiative (ADI)

LOS ANGELES DEPARTMENT OF AGING (LADOA) OFFICIAL CONFLICT OF INTEREST CODE SCHEDULE "A" - DESIGNATED POSITIONS

Nebraska Lifespan Respite Caregiver Survey

Changing Relationships: You and Your Aging Parent/Relative

3 Questions When Looking at Senior Care Options

A Policy Conversation on Family Caregiving for Older Adults

The Impact of an Application of Telerehabilitation Technology on Caregiver Burden

RNAO Delirium, Dementia, and Depression in Older Adults: Assessment and Care. Recommendation Comparison Chart

A Study of Burden and Quality of Life in Caregivers of Person with Severe Mental Illness

11/13/2017. Thank You to Our Sponsors. Evaluations & CE Credits. University at Albany School of Public Health. New York State Department of Health

Quality ID #288: Dementia: Caregiver Education and Support National Quality Strategy Domain: Communication and Care Coordination

REACH II Intervention: Background and Rationale

Background. Population/Intervention(s)/Comparison/Outcome(s) (PICO) Interventions for carers of people with dementia

N4A Annual Conference Philadelphia July 14, The Role of the Family Caregiver and the Aging Network in the Chronic Care Model

Long-Term Services & Supports Feasibility Policy Note

The Important Role of Family Caregivers in Washington State s Long-Term Services and Supports System

Alpert Medical School of Brown University Clinical Psychology Internship Training Program Rotation Description

Family Caregiving. Caregiver Stress and Burnout. Caregiver Tasks. Caregiver Stress and Burnout. Age of Caregivers

Shaping Perceptions of Biopsychosocial Dementia Care with Interprofessional Collaboration DRS. BENJAMIN A. BENSADON & MARÍA ORDÓÑEZ

Chapter Two. Preadmission Screening and Annual Resident Review (PASARR)

From Insight to Advocacy: Addressing Family Caregiving as a National Public Health Issue

Implementation in Health Care and Social Service Systems: REACH VA

Let s talk about Hope. Regional Hospice and Home Care of Western Connecticut

Outside the Box: A. Social Service Model of Community-based Palliative Care. Seniors At Home A division of Jewish Family and Children s Services

Online Interventions for Dementia Family Caregivers: What We Know/What Next?

Innovations in Medicaid Managed Long-Term Services and Supports: How Health Plans are Providing Support to Family Caregivers

The Number of People With Chronic Conditions Is Rapidly Increasing

Edwin Walker. Deputy Assistant Secretary for Aging

Lisa Hee (QUT) Lecturer Post Graduate Aged care coordinator PHD candidate

Training To Serve People With Dementia Is our health care system ready?

Caregiver Assessment (Part I of II): Why and What Should We Assess? Edrena Harrison

Nebraska Lifespan Respite Network

ADULT LONG-TERM CARE SERVICES

Valuing the Costs of Family Caregiving: Time and Motion Survey Estimates

CRISIS SUPPORT TEAMS (CST)

In Solidarity, Paul Pecorale Second Vice President

Measuring self-efficacy for caregiving of caregivers of patients with palliative care need: Validation of the Caregiver Inventory

Section I: Background Section II: Analysis Health Impact of Alzheimer's Disease in Texas Economic Impact of Alzheimer's Disease

Department of Elder Affairs Programs and Services Handbook Chapter 3: Description of DOEA Coordination with other State/Federal Programs CHAPTER 3

Caring for Your Aging Parents

Overview. Improving Chronic Care: Integrating Mental Health and Physical Health Care in State Programs. Mental Health Spending

GERIATRIC SERVICES CAPACITY ASSESSMENT DOMAIN 4 ALTERNATE LIVING ARRANGEMENTS

Is It Time for In-Home Care?

Hospice Care For Dementia and Alzheimers Patients

16 th Annual National Lifespan Respite Conference October 7-8, Nashville TN Brenda Reece, Executive Director High Country Caregiver Foundation

Is It Time for In-Home Care?

Faculty/Presenter Disclosure

Services for Caregivers

The complexity of caring (Part 1): Detrimental health and well-being outcomes for caregivers of people with chronic wounds

Chronic Care Management Services: Advantages for Your Practices

A Journey from Evidence to Impact

People diagnosed with Alzheimer s disease (AD)

Department of Elder Affairs Programs and Services Handbook Chapter 3: Description of DOEA Coordination with Other State/Federal Programs CHAPTER 3

NCPOP Report Launch Family Carers of Older People: Results of a National Survey of Stress, Conflict and Coping

January 4, Via Electronic Mail to file code CMS-3317-P

The Alzheimer Society of Ireland Pre-Budget Submission 2017

Organization: Solution Title: Program/Project Description, including Goals: What is this project? Why is this project important?

Respite Partnership Collaborative Proposers Conference August 30, Sacramento County

Caring for Your Aging Parents

The Development of a Holisitic Dementia Caregiver Program. Karen S. Howell, PhD, OTR/L, FAOTA Kayla Collins, MOT

The Experience of Unpaid Caregivers of Persons Diagnosed with Early- Stage Dementia of the Alzheimer s Type: Embracing Unpredictability

Carers Checklist. An outcome measure for people with dementia and their carers. Claire Hodgson Irene Higginson Peter Jefferys

Jeffrey B. Klein, FACHE President & CEO

Increasing Self-care Ativities for Caregivers of Persons with Alzheimer s Disease and Other Dementias to Reduce Burden and Depression

The economic value of informal mental health caring in Australia

State of California-Health and Human Services Agency EDMUND G. BROWN JR. GOVERNOR

Home Alone: Family Caregivers Providing Complex Chronic Care

Caring for Carers. Includes Caregiver Health Checklists

Coverage of Behavioral Health Services for Children, Youth, and Young Adults with Significant Mental Health Conditions

Updates from the UCSF Health Workforce Research Center

Department of Health and Social Services Division of Services for Aging and Adults with Physical Disabilities. Respite Summit 2015

SOCIAL WORKER III. Merit System Services CLASSIFICATION DEFINITION

Role Play as a Method of Improving Communication Skills of Professionals Working with Clients in Institutionalized Care a Literature Review

Passport Advantage (HMO SNP) Model of Care Training (Providers)

MEDICARE COVERAGE SUMMARY: OUTPATIENT PSYCHIATRIC AND PSYCHOLOGICAL SERVICES

HELPING RURAL COMMUNITIES IDENTIFY RESOURCES FOR THE TERMINALLY ILL. J. P. Burnham Lea Drawdy Elizabeth Pierson

Who are caregivers? What is caregiving? Webster s Dictionary persons who provide direct care to another individual

A Family Caregiver s Guide to Hospital Discharge Planning

CARING for a disabled older person is one of the most

Transcription:

Caring for the Caregiver: Dementia Laura Ruhle BA, CT Health Educator Alzheimer s Association-Greater Michigan Chapter

Geriatric Education Center of Michigan activities are supported by a grant from the U.S. Department of Health and Human Services, Health Resources and Services Administration, Public Health Service Act, Title VII, Section 753(a).

Learning Objectives 1. Describe the therapeutic relationship among the care recipient, caregiver and health care professionals (Triadic Model of Caregiving) 2. Identify the unique challenges inherent in providing care for individuals with dementia (caregiver vulnerability factors) 3. Recognize caregiver strengths and challenges 4. Identify community-based and online resources for caregivers of individuals with dementia

Alzheimer s Association Fact Sheet 2011 In 2010, 14.9 million family and friends provided 17 billion hours of unpaid care to those with Alzheimer s and other dementias. The economic value of the unpaid care provided to those with Alzheimer s and other dementias totaled $202.6 billion in 2010. More than 60 percent of Alzheimer s and dementia caregivers rate the emotional stress of caregiving as high or very high; one-third report symptoms of depression.

Alzheimer s Association Fact Sheet 2011 Between now and 2050, Medicare spending on those with Alzheimer s will increase nearly 600 percent Medicaid spending will increase nearly 400 percent

The Facts about Caregiving Emerging public health issue Life expectancy has increased Caregivers responsibilities are complex and in constant fluctuation Communities are affected by the burdens and practicalities of caregiving Caregiving affects the quality of life for all of us

Triadic Model of Caregiving Identifies the strengths and needs of all in relationship to quality care Brings to light the need for dedication, respect and value to the care experience Allows for recognition of current realities and projects to the future Engages people and societies, politically and scientifically, to seek answers to the complexities of life

Triadic Model of Caregiving

Caregiver Vulnerability Factors Alzheimer s Associations Fact Sheet 2011 One-fourth of women caregivers experience health problems due to the stress associated with caregiving Higher levels of depressive symptoms and mental health problems Two-thirds of caregivers report they need to find support for themselves for mental, emotional and physical balance within the care circle and responsibilities

Zarit Burden Interview A structured caregiver assessment tool using verbal interaction to evaluate levels of stress in family members or caregivers of Alzheimer patients.

Zarit Burden Interview On-going assessment process Identifies that the disease is a family affair Validates the people in the experience

Zarit Burden Interview Assists in using more time/resources more efficiently Guides conversation and collects vital information for the evolving Plan of Care Identifies changing progress and needs

Support Interventions National Family Caregiver Support Program Informs caregivers about available services Assists caregivers in gaining access to services needed Provides individual support and counseling Assists with respite care http://www.aoa.gov/aoaroot/aroa_programs/hcltc/caregiver/index/aspx

Support Interventions Family Caregiver Alliance Online Toolkit to Assist Practitioners Assess the Needs of Family Caregivers http://www.caregiver.org

Support Interventions The Savvy Caregiver Psychoeducation Evidence-based Program Provides the foundational understanding/living with a Dementia disease process Identifies the on-going changes and how they can effect caregivers Strengthens the managing of daily living with AD Assists with identifying the need for Critical Decision-Making Validates the importance of Taking Care of Oneself Links participants with area resources

Support Interventions Alzheimer s Association 1-800-272-3900 www.alz.org Harry L. Nelson Helpline 24/7 Information and referral Care Consultation Support Groups MedicAlert/Safe Return/Comfort Zone Education Programs and Workshops

Support Interventions the key to quality support intervention is to find and combine the unique variety of services that address the needs of the particular caregiving situation

Caregiving is Interactional process marked by constant change in one s world which disables one and demands for another Requires familial and social support for the well-being of all affected by Dementia

As they say, If only I knew what I know now. - And Thou Shalt Honor The Caregiver s Companion 2002

Supplemental Resources Hepburn, K., Lewis, M., Tornator, J., C.W., Lindstrom Bremer, K. (2007). The savvy caregiver. Journal of Gerontological Nursing, 30-36. Lee, B. (2007) Caregiving: A far-reaching public health concern. American Journal of Public Health. Retrieved 3 August, 2011 from: http://ajph.aphapublications.org/cgi/content/full/97/11/1931. Mittelman, M.S., Haley, W.D., Clay, O.J. Roth, D.L. (2006). Improving caregiver well-being delays nursing home placement of patients with Alzheimer Disease. Neurology, 6, 1592-1599. Schulz, R., O Brien, A.T., Bookwala, J., Fleissner, K. (1995). Psychiatric and Physical mnorbidity effects of dementia caregiving: Prevalence correlates and causes. The Gerontologist, 35, 771-791.

Supplemental Resources Talley, R.C. & Crews, J.E. (2006). Caring for the most vulnerable: Framing the public health of caregiving. American Journal of Public Health, 97, 224-228. Whittier, S., Coon, D., Aker, J. (2001). Caregivier support interventions. In Scharlash, A. et al., eds. In : Family Caregiver California: Neds, Interventions, Family Programs. University of California at Berkeley. Center for the Advanced Study of Aging Services. School of Social Welfare. Zarit, S.J., Reever, K.E., Bach-Pterson, J. (1980). The burden interview. The Gerontologist 20, 649-655.