Many people are caring for a chronically ill or disabled spouse, parent, or other family member. Caregiving can be a rewarding experience, especially when you know that your care makes a positive difference. But caregiving can be difficult. There are three tips to being a good caregiver:
This topic will tell you more about these tips and how they can help both you and the person you are caring for.

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Taking care of yourself is your most important step as a caregiver. Caregivers are more likely than those who are not caregivers to be at risk for colds and the flu and also chronic illness, such as heart disease, diabetes, and cancer.1
On the other hand, when caregivers take time to care for themselves, good things usually happen:
Here are some important things that you need to find time to do—just for yourself:
Even if they don't admit it, people like to help themselves. Every time you do something for a person that the person could have done without help, there is a double loss. First, your effort may have been wasted. Second, the person has missed an opportunity to help himself or herself.
As a caregiver, your highest goal is to give the person you are caring for the power and the permission to be in control of his or her own life (as much as possible). Every act your loved one makes to maintain independence is a victory for you as a caregiver.
Here are some things you can do to empower the person you are caring for to do things independently:
The best answer to the question, “Is there anything you need?” is “Yes.”
"Yes, I need someone to stay here so I can go out." Or "Yes, I could really use a nap." Letting others help can make your caregiving easier. Know where to find help when you need it. The more support you have, the more successful you are likely to be.
When family or friends offer to lend a hand, be ready with specific ideas. Let them pick something they would like to do. For example, you could ask them to:
There are other ways to find support, for example:
Services that may be useful to caregivers include the following:
Respite care may be the most important service for caregivers. Respite services provide someone who will stay with the person while you get out of the house for a few hours. If the person you are caring for needs routine medical care, you may be able to arrange to have the person stay in a nursing home for a few days while you get away for a break.
Adult day centers are "drop-off" sites where a person who does not need individual supervision can stay during the day. This service is usually offered during working hours and may or may not be available on weekends. Meals, personal care services, and social activities are provided.
Adult foster care or board-and-care homes are private homes where older adults receive around-the-clock personal care, supervision, and meals. Some states require board-and-care homes to be licensed.
Nursing homes generally have two levels of care. Intermediate care includes assistance with using the toilet, dressing, and personal care for people who do not have serious medical conditions. Skilled nursing care is usually for people who have just come from the hospital or for others who have medical conditions that require more intensive nursing care. Some facilities have special units for people with dementia.
Hospice programs provide social, personal, and medical services for terminally ill people who wish to spend their remaining time at home or in an environment less formal than a hospital or nursing home.
Support groups give you a chance to discuss problems or concerns about caregiving with other caregivers.
To learn whether these services are available in your community, look under "Senior Citizen Services" in the Yellow Pages.
Take pride in your efforts. Being a caregiver is not easy, and those who do it are special. Following the tips for caregiving can help you feel good about yourself and the care you provide. Remember:
| Family Caregiver Alliance | |
| 180 Montgomery Street | |
| Suite 1100 | |
| San Francisco, CA 94104 | |
| Phone: | 1-800-445-8106 (415) 434-3388 |
| Email: | info@caregiver.org |
| Web Address: | www.caregiver.org |
This organization supports and assists people who are providing long-term care at home. It also provides education, research, services, and advocacy. | |
| National Family Caregiver Support Program | |
| U.S. Department of Health and Human Services | |
| Suite Administration on Aging | |
| Washington, DC 20201 | |
| Phone: | (202) 401-4634 |
| Fax: | (202) 357-3555 |
| Email: | aoainfo@aoa.gov |
| Web Address: | www.aoa.gov/AoARoot/AoA_Programs/HCLTC/Caregiver/index.aspx |
This Web site is for caregivers and families. It offers many caregiving resources, including where to find help, ways to take care of others and yourself, how to join a caregiver support group, and more. There are links to information about and help for finding support services in your community. | |
| National Family Caregivers Association | |
| 10400 Connecticut Avenue | |
| Suite 500 | |
| Kensington, MD 20895-3944 | |
| Phone: | 1-800-896-3650 (301) 942-6430 |
| Fax: | (301) 942-2302 |
| Email: | info@thefamilycaregiver.org |
| Web Address: | www.nfcacares.org |
The National Family Caregivers Association (NFCA) educates, supports, empowers, and speaks up for the more than 50 million Americans who care for loved ones with a chronic illness or disability or the frailties of old age. NFCA reaches across the boundaries of diagnoses, relationships, and life stages to address the common needs and concerns of all family caregivers. | |
Citations
- Administration on Aging (2005). Caregiver Tip Sheet. Washington, DC: U.S. Department of Health and Human Services. Available online: http://www.aoa.gov/prof/aoaprog/caregiver/overview/docs/CaregiverTipSheet.pdf.
- U.S. Department of Health and Human Services (2008). 2008 Physical Activity Guidelines for Americans (ODPHP Publication No. U0036). Washington, DC: U.S. Government Printing Office. Available online: http://www.health.gov/paguidelines/pdf/paguide.pdf.
Other Works Consulted
- Boal J, Loengard A (2007). Home care. In RJ Ham et al., eds., Primary Care Geriatrics: A Case-Based Approach, 5th ed., pp. 172–177. Philadelphia: Mosby Elsevier.
- Family Caregiver Alliance (2003). Fact Sheet: Taking Care of YOU: Self-Care for Family Caregivers. Available online: http://www.caregiver.org/caregiver/jsp/print_friendly.jsp?nodeid=847.
- Family Caregiver Alliance (2004). Fact Sheet: Caring for Adults with Cognitive and Memory Impairments. Available online: http://www.caregiver.org/caregiver/jsp/print_friendly.jsp?nodeid=392.
- Family Caregiver Alliance (accessed November 2008). A Guide to Taking Care of Yourself. Available online: http://www.caregiver.org/caregiver/jsp/print_friendly.jsp?nodeid=667.
- Goldstein NE, Morrison RS (2007). Palliative care. In RJ Ham et al., eds., Primary Care Geriatrics: A Case-Based Approach, 5th ed., pp. 194–205. Philadelphia: Mosby Elsevier.
- Joberst GJ, Wilbur JK (2007). Care of the elderly. In RE Rakel, ed., Textbook of Family Medicine, 7th ed., pp. 67–105. Philadelphia: Saunders Elsevier.
- Nusbaum NJ (2007). Rehabilitation. In RJ Ham et al., eds., Primary Care Geriatrics: A Case-Based Approach, 5th ed., pp. 179–193. Philadelphia: Mosby Elsevier.
- Pinquart M, Sörensen S (2007). Correlates of physical health of informal caregivers: A meta-analysis. Journals of Gerontology, 62B(2): 126–137.
- Rakel RE, Storey P (2007). Care of the dying patient. In RE Rakel, ed., Textbook of Family Medicine, 7th ed., pp. 107–126. Philadelphia: Saunders Elsevier.
- Vitaliano PP, et al. (2003). Is caregiving hazardous to one’s physical health? A meta-analysis. Psychological Bulletin, 129(6): 946–972.
| By | Healthwise Staff |
|---|---|
| Primary Medical Reviewer | Kathleen Romito, MD - Family Medicine |
| Specialist Medical Reviewer | Adam Husney, MD, MD - Family Medicine |
| Specialist Medical Reviewer | Anne C. Poinier, MD - Internal Medicine |
| Last Revised | December 9, 2010 |
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ReferencesLast Revised: December 9, 2010
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