A family caregiver decision guide. Caregiving at home for someone with life-limiting illness

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A family caregiver decision guide Caregiving at home for someone with life-limiting illness

Things change and this decision guide can be used over and over. Here s a place to keep track when you use the guide. This guide is the property of the family. First completed on this date:. Reviewed a second time on this date:. Reviewed a third time on this date:. Last completed on this date:. (Some people find it helpful to use a different color each time they complete the guide.) You may reproduce the Family Caregiver Decision Guide for your own use (not for sale or distribution without permission). For further information regarding this guide and training for its use contact Dr. Carole Robinson at carole.robinson@ubc.ca or by telephone at 250-807-9882. Acknowledgements The team sincerely thanks all the families who participated in the research to create this guide. We would also like to thank Natalia Polchenko, Laura Bissell, and Janelle Zerr for their valuable contributions. Funding support for the guide was provided by Interior Health in partnership with the Institute for Healthy Living and Chronic Disease Prevention at The University of British Columbia Okanagan campus, as well as the British Columbia Cancer Foundation. Suggested citation Robinson, C.A., Pesut, B., & Bottorff, J.L. (2015). A family caregiver decision guide. Kelowna, BC: University of British Columbia. ISBN: 978-0-88865-158-7 Robinson, C.A., Pesut, B., Bottorff, J.L. 2015 1 A family caregiver decision guide

This decision guide is for me, if: My family member is living with a life-limiting illness I would like to plan for possible changes in needs for caregiving for my family member. Providing care for a family member is a process that often changes, sometimes quite suddenly. You may provide more care over time alone, or with help from others. Careful planning allows you to care for your family member at home for as long as possible if you choose to do so. This guide will help you with this plan. You will be guided through four steps to help you with your decision planning: Think about my caregiving situation now. 1 2 Think about how my caregiving situation might need to change. 3 Explore caregiving options in my area. Not all parts of this guide will apply to you today. Focus on the parts that are important to you right now and finish the other parts that may be more relevant to you later on. It may be useful to complete this guide one step at a time or over several days. Revisit it when needs for caregiving change. Once you have completed this guide, talk it over with a health care provider to answer any questions or needs that may arise. Some people may want to complete the guide with a nurse or volunteer. What are my best options if the needs for caregiving change? 4 2

1 Think about my caregiving situation now. How am I managing with... Home maintenance: Inside Outside Car maintenance Grocery shopping Cooking Taking care of pets Home changes for safety and convenience (e.g., wheelchair ramps, grab bars in the bathroom etc.) Getting special equipment (e.g., walker, hospital bed, commode, wheelchair) Personal care of your loved one: Bathing Toileting Dressing Transferring in and out of bed Managing incontinence of bowel and/or bladder Wound care I do not need help I could use some help Continued on next page... 3 A family caregiver decision guide

Continued from previous page... I do not need help I could use some help My family member s : Pain control Symptom management (e.g., constipation, nausea and vomiting, breathlessness, confusion, trouble swallowing) Medications (e.g., giving and keeping a record) Transportation to and from healthcare appointments Knowing the signs and symptoms of a problem that requires medical attention Helping my family member stay involved in meaningful activities Helping my family member stay active 4

How confident am I with I AM okay now I could use some help I May Need help in future Understanding the illness now Understanding how the illness is likely to change over time Understanding changes that might require medical attention Understanding the goals of treatment Recognizing when end of life is approaching Talking with my family member about the illness, how it may change, and plans for care Understanding my family member s wishes for care: Now Towards end-of-life (e.g., goals of care, advance care plan, resuscitation orders) Overall, how well am I managing caregiving now? Please, place an X on the line to show how well you are managing: Poorly Very well 5 A family caregiver decision guide

What might be helpful to maintain my health so that I can provide the best care for my family member? Financial support (e.g., income replacement, palliative benefits, employee assistance) Legal support (e.g., representation agreement for health care decision making, Power of Attorney, will) Emotional support (e.g., counselling) Religious or spiritual support Getting some time for myself Breaks from caregiving (respite): In the home Outside the home Doing meaningful things Keeping active Other (specify): I am doing Okay I could use more of this 6

2 Think about how caregiving might need to change either now or in the future. It s important to think about how your caregiving will change, because it will! Being a caregiver you have to make choices it s challenging. And when needs change over time, it s important to revisit your options. Planning in advance is a good idea. But sometimes you can t predict what will happen. As things change it is important to ask yourself if you can maintain the care you want to give. (Family caregiver) Have you thought about the choices you might have to make? Yes No What would tell me that I cannot keep caregiving at home any longer? Tick all that apply. Cannot keep up with important tasks My own health is worsening My family member s pain becomes unmanageable at home My family member s symptoms are getting unmanageable at home Exhaustion Mixed emotions about living in the home after death Other (specify): 7 A family caregiver decision guide

What things influence me when it comes to making choices about caregiving for my family member? Tick all that apply. Beliefs about what is right Desire to spend time with my family member Lack of information about options, pros and cons Views of other family members about the care that is needed Feeling pressure from others Available support from family or friends Available support from healthcare providers Lack of understanding about how the illness will go Comfort and privacy of home My family member s wishes to stay at home My family member s wishes to be cared for by me Promise for family member to stay at home until death Other (specify): 8

What things influence my family member when it comes to making choices about their care? Tick all that apply. Beliefs about what is right Desire to spend time with family Lack of information about options, pros and cons Feeling pressure from others Available support from family or friends Available support from healthcare providers Lack of understanding about how the illness will go Comfort and privacy of home Desire to stay at home Desire to be cared for by me Desire not to be a burden Other (specify): I am unclear about what is most important to them Who else is involved in caregiving for my family member? Who is this person (name)? What role does this person play in providing care? 1. 2. 3. 4. 5. 9 A family caregiver decision guide

3 Explore caregiving options in my area. Do I know what supports are available to me? Are the following resources available in my area? Yes No Don t Know Food and meal services Pet care services Housekeeping services Recreation programs Medical equipment & supplies Transportation Support for specific conditions (e.g., cancer) Programs to give you a break from caregiving Volunteers (e.g., hospice or community services) Physiotherapy Medication management and delivery (e.g., pharmacies) Personal care for my family member 10

4 What are my best options if the needs for caregiving change? Respite* is a short period of rest and relief for caregivers. Respite can be provided in the community through Adult Day Services or in a residential care facility on a short-term basis or in a hospice. Health Care Facility** could mean a hospital, long term care facility, palliative care facility, or hospice. How do I feel about these caregiving options? Home with increased resources I really dislike this option My reasons: 1 2 3 4 5 Home with respite* away from home I really like this option I really dislike this option 1 2 3 4 5 I really like this option My reasons: Health care facility** I really dislike this option 1 2 3 4 5 I really like this option My reasons: 11 A family caregiver decision guide

How does my family member feel about these caregiving options? Home with increased resources Really dislikes this option Their reasons: 1 2 3 4 5 Really likes this option Considering everything I know... What is my best option if the needs for caregiving change and I can no longer keep caring at home with the resources available to me? Home with respite* away from home Really dislikes this option Their reasons: Health care facility** 1 2 3 4 5 Really likes this option Home with increased resources Home with respite away from home Health care facility Hospital Care Home Hospice Other (specify): Really dislikes this option 1 2 3 4 5 Really likes this option Their reasons: 12

Ask yourself... What do I need to do now so I can continue caregiving? What do I need to do now to prepare for future changes in caregiving? 13 A family caregiver decision guide

What questions do I have for a family doctor or other health care professional (e.g., community or palliative nurse) about caring at home? What questions do I have for a family doctor or other health care professional about alternative places of care (e.g., Health Care Facility)? 14

Contact Information Who can I contact for help if the needs for caregiving change? Family Doctor: Health Care Agencies (e.g., home care, community nursing, hospice or palliative care, Red Cross equipment loan services, Meals on Wheels): Family: Friends: Religious or Spiritual Leader: Lawyer or Notary: Banker: Other (specify): 15 A family caregiver decision guide

Notes 16

Resources Advance Care Planning Speak Up www.advancecareplanning.ca Family Caregiver Resources Aging Parents Canada www.agingparentscanada.ca Canadian Caregiver Coalition www.ccc-ccan.ca Select the Resources tab Caregiving.com www.caregiving.com The Family Caregiver www.thefamilycaregiver.com 1-800-209-4810 Canadian Mental Health Association www.cmha.ca Hospice/Palliative Care American College of Physicians Home Care Guide for Advanced Cancer www.acponline.org/patients_families/end_of_life_issues/ US site that has valuable resources for family, friends and hospice workers when caring for individuals with advanced cancer at home Canadian Virtual Hospice www.virtualhospice.ca Canadian Hospice Palliative Care Association www.chpca.net Select Family Caregiver tab 1-800-668-2785 Family Caregiving for People at the End of Life www.eolcaregiver.com There is a great resource link on the home page Family Hospice Care www.legacies.ca Victoria Hospice www.victoriahospice.org Select the How we can help you tab 17 A family caregiver decision guide

Government Assistance Canada Benefits www.canadabenefits.gc.ca Go to the middle section under Life Events then Dealing with death Health Canada Palliative and End-of-Life Care www.hc-sc.gc.ca/hcs-sss/palliat/index-eng.php Employment Insurance (EI) Compassionate Care Benefits www.servicecanada.gc.ca/eng/ei/types/compassionate_care.shtml 1-800-622-623 Grief and Bereavement Support AfterGiving - When Caregiving Ends, Beginning New www.aftergiving.com Bereavement Self Help Resources www.bereavement.ca Compassion Books www.compassionbooks.com 1-828-675-5909 GriefNet www.griefnet.org Journey of Hearts www.journeyofhearts.org Kidsaid 2 Kids, 4 Kids, by Kids www.kidsaid.com Information on Specific Illnesses ALS Society of Canada www.als.ca 1-800-267-4257 Alzheimer Society of Canada www.alzheimer.ca 1-800-616-8816 Canadian AIDS Society www.cdnaids.ca 1-800-499-1986 Canadian Cancer Society www.cancer.ca 1-888-939-3333 Cancerview www.cancerview.ca Link to Resources for Patients and Families on the home page Excellent Caregiver video link in The Truth of It series Cancer Chat Canada www.cancerchatcanada.ca 1-877-360-1665 1-877-547-3777 ext. 645234 Canadian Diabetes Association www.diabetes.ca Canadian Lung Association www.lung.ca/home-accueil_e.php Education and resource materials under Lung Health tab Heart and Stroke Foundation of Canada www.heartandstroke.ca Kidney Foundation of Canada www.kidney.ca 1-800-361-7494 Leukemia and Lymphoma Society of Canada www.lls.org/canada 1-800-955-4572 National Cancer Institute www.cancer.gov US site, but provides information internationally as well. 1-800-422-6237 Mon-Fri 8am-8pm ET 18

For more information regarding this guide: Contact Dr. Carole Robinson at carole.robinson@ubc.ca or by telephone at 250-807-9882 19