Family caregivers

Family caregivers (also known as “carers”) are “relatives, friends, or neighbors who provide assistance related to an underlying physical or mental disability but who are unpaid for those services.” [1]

See also: Caregiver, Carers rights movement, Caregiving and dementia, and Long-term care

A recent study says that 26.5% of all American adults today are family caregivers.[2] A 2012 report by the Alzheimer’s Association states that 15 million of those family caregivers are caring for a person with Alzheimer’s disease or another dementia.[3] The value of the voluntary, "unpaid" caregiving service provided by caregivers was estimated at $310 billion in 2006 — almost twice as much as was actually spent on home care and nursing services combined.[2] By 2009, about 61.6 million caregivers were providing "unpaid" care at a value that had increased to an estimated $450 billion.[4] It is projected that nearly one in five United States citizens will be 65 years of age or older by the year 2030. By 2050 this older population is expected to double in size.[5]

Family caregiver experience

A 2011 survey of family caregivers in the United States found that almost half (46%) take on tasks that are traditionally considered “nursing” or “medical,” such as injections, wound care, and operating medical equipment and monitors.[6] While the family caregivers’ assumption of such responsibilities is not new, the frequency may have increased over time due to shorter hospital stays, adults living longer with significant ailments, and technological and health care improvements allowing more nursing or medical care to be provided at home. This trend has implications for families, patients, family caregivers’ workplaces, health care organizations, and insurers, including Medicare and Medicaid. A survey by AARP in 2010 states that "29% of the U.S. adult population, or 65.7 million people, are caregivers, including 31% of all households. These caregivers provide an average of 20 hours of care per week."[7]

1.4 million children ages 8 to 18 provide care for an adult relative; 72% are caring for a parent or grandparent. Fortunately, most are not the sole caregiver.[8] 30% of family caregivers caring for seniors are themselves aged 65 or over; another 15% are between the ages of 45 to 54.[9]

Caregiver gain

As discussed above, there are benefits to the caregiving experience. New research even reports gains in cognitive function in older women who provide informal (unpaid) care on a continuing basis.[10] This cross-sectional study tested over 900 participants at baseline and again after two years for memory and processing speed, functions which are necessary for many caregiving tasks. The participants were divided into three groups, those who were caregivers over the entire two-year period, those who were caregivers at the start of the study but not at the two-year follow-up, and those who were not caregivers at any time during the research period. At follow-up, those who were caregivers throughout the study had the highest scores for both cognitive functions but also the highest reported levels of stress, while those participants who were not caregivers at any time during the study had the lowest scores for both cognitive functions and the lowest reported levels of stress. These results are consistent with the healthy caregiver hypothesis which states that while those older adults who are more likely to be caregivers are healthier to start with, it is the work of caregiving that helps keep them healthier than older adults who are not caregivers. This model contrasts with the long-held idea that the stress of caregiving results in poorer functioning over time.

In contrast, subsequent research[11] has found that the benefit to family caregivers varies depending on the health of the person receiving care. Higher numbers of chronic conditions among those receiving care were associated with increased job stress, concern over making harmful errors, hypervigilance, feelings of depression, and feelings of suboptimal health among family caregivers. Nevertheless, family caregivers reported that they felt emotionally closer to the care recipient and that they were making a positive contribution to the care recipient’s life. In addition, training in medical and nursing tasks was found to have a protective effect for the family caregiver. Research has also found that most family caregivers said they had not received training about medication management from a professional, but rather had learned it on their own. In addition to this, optimism significantly mediated some of the relationship between angry reaction and vitality[12].

Taking care of the caregiver

One of the most common negative outcomes of being a caretaker is the infringement on time and activities. In most cases, this role becomes a full-time job in itself and does not leave much time for leisure activities the caregiver liked to participate in before becoming a primary caregiver. While this seems like an obvious outcome of caregiving, it is a critical cause of depression and if steps are not taken to intervene and provide the primary caretaker with adequate off time then they will quickly become not only depressed but resentful of their role as well [13] Other negative outcomes of being an informal primary caregiver can include an unfavorable relationship forming between the caregiver and receiver dyad as well as declines in both physical and mental health of the caregiver. wide variety of health issues that arise from being a primary caregiver. They reported that when caregivers were compared to equal non-caregivers, they were found to have a 15% lower level of antibody response and a 23% higher level of stress hormones in their bodies. This indicates the stress and strain placed upon primary caregivers can greatly impact their health and ability to recover from illness themselves.[14] There are, however, strategies that caregivers and communities can use to reduce the effects of this added stress. Providing a type of respite care is the easiest intervention to reduce this negative outcome. It varies in forms, but the basic principle of respite care is to provide temporary care for a care recipient when their primary caregiver must be absent. It can be as informal as sitting with someone while the caregiver runs errands to a more formal setting such as an Adult Day Service or even overnight stay in an hospital or nursing home facility.[15] Information, resources and support are often available through senior centers and local public health departments, but more research is needed to determine what services are helpful. Two studies that investigated the effectiveness of different interventions on the health of caregivers are described below.

The Resources for Enhancing Alzheimer's Caregiver Health (REACH) II intervention[16] was a randomized clinical trial that provided self-care educational information and training on self-care skills, tailored to each caregiver's needs, to the intervention group, or a basic health information packet and two non-educational phone calls to the control group. Each intervention was designed to deal with a participant's personal issues using information provided by the caregiver at the beginning of the study, and researchers were personally involved during the 12 face-to-face and telephone sessions. At the end of the six-month study period, those receiving the intervention reported better physical and emotional health and less "burden and bother" with their caregiving duties than those in the control group.

Another study tested the effectiveness of three different interventions (a support group, provision of literature on self-care and caregiving, and creative movement) on five mental health variables of caregiving daughters of frail mothers.[17] Each study participant chose the intervention that appealed to her most, rather than being randomly assigned to one. Study participants were then evaluated for self-reported irritability, depression, anxiety, stress, and concentration, and asked to assess the chosen intervention on an ongoing basis. Comparing the outcomes of the five variables, the support group's self-ratings suggested greater improvement than the literature group while the creative movement group was too small for a meaningful comparison. The participants' assessments of all three interventions were positive, with caregivers using words such as "validation," "reinforcement," and "relaxing." All study participants agreed that they would choose to participate again, and in the same intervention group. Those in the support group found the intervention so helpful that they continued to meet after the study's completion. For caregivers without the ability to join nearby support groups, online support groups such as a caregiver forum can offer similar benefits.

A different study has shown that family caregivers whose loved ones receive round the clock migrant home care services report greater satisfaction with the services, lower levels of burden, higher levels of subjective health and better well-being compared with home care services provided for only several hours per week. This is despite the fact that the group that relied on round the clock migrant home care workers had lower physical functioning.[18]

Signs of caregiver stress

Caregiver stress is the emotional and physical strain of care giving.[19]

Avoiding Caregiver Burnout

Caregiver stress explodes when the caregiver can't get much of a break - whether it is emotional or physical, a needed break is what makes it possible for the caregiver to function. The Be Well Bistro Caregiver's Corner offers strategies to support the caregiver such as:

Tips for avoiding burnout are to know the signs and have a plan in place to combat the burnout. Some signs:

  • Anger or annoyance at all kinds of things[20]
  • Exhaustion
  • Nagging aches and pains
  • Over eating or Loss of appetite
  • Loss of interest in personal goals
  • Loss of joy in doing things once loved
  • Wanting to run away

It happens all too fast. And most caregiver stress can be avoided with a strategy to avoid it. Here are some tips:

  • Enlist family members to pitch in
  • Enlist a friend or a few friends
  • Create a care group so friends, family, or neighbors can coordinate to give the caregiver some respite
  • Think Outsourcing: Make a list of all the chores you don't want to do. Find a way to bring in help. If your family or friends can't or won't help, maybe a local church group, community respite organization. Ask on Facebook if anyone in your community knows someone—or ask a local email group. Think outside the box.
  • Find a local support group where you can meet people in person.
  • Find a Psychotherapeutic intervention[21].

Banish the Negatives

Guilt, Worry and Shame serve no one. You didn't cause this. You can't control it and you can't fix it. Any time you feel these emotions, ask yourself if they are true. They aren't - but ask anyway. You are only one person. You know when you need a break. And when the person receiving care keeps adding on to you already empty reserves of energy, you can't always take it. When that happens, find a way to take a break. A full day off and way is essential. You may need to take your person to an Adult Care Day location—You might need to hire someone to stay at your house. But you have to get away.

Coach Nancy Lamb at the BeWellBistro.com has tons of tips and offers support to others. No one can do this caregiving alone. The isolation is unbearable. She writes for 3 websites and offers workshops, tips, and stress management plans. Caregiving is usually not a planned thing, but a loving person notices things are needed and starts slowly doing them. Caring for elderly parents for 23 years, and then finding herself in a situation where the caregiving just didn't end, Nancy became an unwitting expert in self-preservation while in the throes of caregiving.

Caregiving versus Caretaking

In many dysfunctional groups, there is one person who ends up being the over responsible caretaker who gets their self-esteem from caring for other members. They do too much for others and not enough for themselves. What it means in recovery circles is that the person is doing for others what they can and should be doing for themselves. In the alcoholic work place, people cover for the worker who routinely misses deadlines, comes in late, or gets sick too often. In the alcoholic home, it's the person who cleans up, covers up, calls in sick for another person, or does everything they can to make the home life look normal when it isn't. That is unhealthy caretaking and a learned behavior.

In a Caregiving Home, the lines can be sometimes blurred. It may start slowly when the one needing care may need help after an illness or surgery. The caregiver finds it natural to help. The patient gets used to this help. The challenge for the caregiver is to know where to draw the line. Caregiver's are naturally giving and helpful people. Compassion is their core strength—but they run the risk of caretaking when they do too much for the person. There is a need for balancing caregiving when it is needed with caretaking where it is too much of one person feeling improperly responsible for duties that should be handled by the other person.

National Family Caregivers Month

The United States President proclaims the month of November as National Family Caregivers Month. On October 31, 2017, President Donald Trump proclaimed the month as National Family Caregivers Month.[22][23][24]

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See also

References
  1. Committee on the Future Health Care Workforce for Older Americans, Board on Health Care Services, INSTITUTE OF MEDICINE OF THE NATIONAL ACADEMIES. "RETOOLING FOR AN AGING AMERICA: BUILDING THE HEALTH CARE WORKFORCE". THE NATIONAL ACADEMIES PRESS. Archived from the original on 2011-09-02. Retrieved 2012-10-23.CS1 maint: multiple names: authors list (link)
  2. Peter S. Arno (Fall 2006), Caregiving (presentation)|format= requires |url= (help), NIH Care Coordination and the Caregiving Forum
  3. Alzheimer's Association. "2012 Alzheimer's Disease Facts and Figures" (PDF). Alzheimer’s & Dementia, Volume 8, Issue 2. Archived from the original (PDF) on 2013-05-17. Retrieved 2012-10-23.
  4. Feinberg, L., Reinhard, S., & Choula, R. AARP, Public Policy Institute. (2011). Valuing the invaluable: 2011 update the growing contributions and costs of family caregiving.
  5. [Vincent, G., Velkoff, V. (2010). The next four decades the older population in the United States: 2010 to 2050. U.S. Census Bureau]
  6. Susan C. Reinhard; Carol Levine; Sarah Samis. "Home Alone: Family Caregivers Providing Complex Chronic Care" (PDF). AARP and United Hospital Fund. p. 41. Retrieved 1 October 2012.
  7. "Almost One-Third of U.S. Adult Population Plays Caregiver Role in Hous..." AARP. 2010-03-13. Retrieved 2015-02-18.
  8. National Alliance for Caregiving and the United Hospital Fund (2005), Caregiving (presentation)|format= requires |url= (help), National Alliance for Caregiving and the United Hospital Fund
  9. U.S. Department of Health and Human Services (2001), Caregiving (presentation)|format= requires |url= (help), Rockville: Agency for Healthcare Research and Quality
  10. Bertrand, R.M., Saczynski, J.S., Mezzacappa, C., Hulse, M., Ensrud, K., & Fredman, L. (2011). Caregiving and cognitive function in older women: Evidence for the healthy caregiver hypothesis. Journal of Aging and Health, 24(1), 48-66.
  11. Susan C. Reinhard; Carol Levine; Sarah Samis. "Home Alone: Family Caregivers Providing Complex Chronic Care". AARP and United Hospital Fund. p. 41. Retrieved 1 October 2012.
  12. López, J.; Romero-Moreno, R.; Márquez-González, M.; Losada, A. (2015). "Anger and Health in Dementia Caregivers: Exploring the Mediation Effect of Optimism: Optimism Mediation". Stress and Health. 31 (2): 158–165. doi:10.1002/smi.2539.
  13. [Montgomery, R., Rowe, J., & Kosloski, K. (2007). Handbook of gerontology: Evidence-based approaches to theory, practice, and policy. (pp. 426-430). Hoboken, NJ: John Wiley & Sons, Inc.]
  14. [Vitaliano, P., Young, H., & Zhang, J. (2004). Is caregiving a risk factor for illness. Current Directions in Psychological Science, 13(1).]
  15. [Sultz, H. A., & Young, K. M. (2011). Health care USA. (7th ed.). Sudbury, MA: Jones & Bartlett Publishers.]
  16. Elliott, A.F., Burgio, L.D., & DeCoster, J. (2010). Enhancing caregiver health: Findings from the Resources for Enhancing Alzheimer's Caregiver Health II intervention. Journal of the American Geriatrics Society, 58, 30-37.
  17. Donorfio, L.K.M., Vetter, R., & Vracevic, M. (2010). Effects of three caregiver interventions: Support, educational literature, and creative movement. Journal of Women and Aging, 22, 61-75.
  18. Ayalon, Liat; Green, O. (2013). "Live-In Versus Live-Out Home Care in Israel: Satisfaction With Services and Caregivers' Outcomes". Gerontologist. 55 (4): 628–642. doi:10.1093/geront/gnt122.
  19. "Caregiver stress fact sheet". womenshealth.gov. Archived from the original on 2014-08-01. Retrieved 2015-02-18.
  20. Márquez-González, María; López, Javier; Romero-Moreno, Rosa; Losada, Andrés (2012). "Anger, Spiritual Meaning and Support from the Religious Community in Dementia Caregiving". Journal of Religion and Health. 51 (1): 179–186. doi:10.1007/s10943-010-9362-7. ISSN 0022-4197.
  21. López, Javier; Crespo, María (2008). "Analysis of the efficacy of a psychotherapeutic program to improve the emotional status of caregivers of elderly dependent relatives". Aging & Mental Health. 12 (4): 451–461. doi:10.1080/13607860802224292. hdl:10637/6749. ISSN 1360-7863.
  22. Office of the Press Secretary (October 31, 2017). "President Donald J. Trump Proclaims November 2017 as National Family Caregivers Month". whitehouse.gov. Washington, D.C.: White House. Retrieved November 6, 2017.
  23. "2017 Health Observance Dates". National Hospice and Palliative Care Organization. Alexandria, Virginia : NHPCO, LLC. Retrieved November 6, 2017.
  24. "National Family Caregivers Month, 2017". Federal Register. Washington, D.C.: National Archives and Records Administration. October 31, 2017. Archived from the original on November 6, 2017. Retrieved November 6, 2017. Alt URL
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