Providing care for a loved one diagnosed with a serious illness can pose significant challenges, but there are steps you can take to make it an enlightening journey.
By John Leifer
For many of us, life flows unabated until certain events intrude and turn our world upside down. It may be a diagnosis of cancer in a close family member, the early signs of Alzheimer’s in an aging parent, or perhaps the heart-breaking realization that a child has a chronic condition that will require a lifetime of care. In such moments our roles and reality change in an instant. We become caregivers.
It happened to Darrell H. more than 20 years ago. A Methodist pastor, whose reflective manner communicates the profound depth of his faith, Darrell says specialists spent more than two years debating the underlying cause of his wife, Patricia’s, odd constellation of symptoms. Then, in November 1993, they finally reached a consensus: Patricia had an unusual form of lymphoma.
But the difficult news did not stop there. At the same time that Darrell and Patricia had been struggling to determine the source of her symptoms, they were desperately seeking an explanation for the apparent delayed development of their daughter, Meghan. Within 24 hours of Patricia’s diagnosis, Meghan was diagnosed with severe autism.
However he defined himself before those fateful events, Darrell was now, first and foremost, a caregiver. It was a “new normal” with profound ramifications—a revised reality that had the capacity to bring both great joy and deep sorrow. It’s a role that would shape two decades of his life with Patricia, before lymphoma ultimately claimed her, and a lifetime with Meghan. It was also a role that would challenge his faith to the core yet lead him to emerge stronger and with deeper conviction.
The Growing Ranks of Caregivers
Darrell’s story is not unique. According to the National Alliance for Caregiving, there are currently more than 65 million Americans serving as caregivers. That number is forecast to grow steeply based on two seemingly immutable trends: our aging population and the transformation of our healthcare delivery system.
Decades ago a prescient writer named Ken Dychtwald warned that, as baby boomers began to age, a virtual tsunami of older Americans would one day overwhelm the healthcare system. He termed this phenomenon the age wave.1 Today more than 10,000 baby boomers turn 65 on a daily basis, and the impact is proving profound: “Over the past 20 years, there has been a rise in chronic disease prevalence, and the majority of the older population, over age 65, now suffers from multiple chronic diseases,” according to researcher William Hung.2
The effects of the tsunami are dramatically intensified by a healthcare system that has divorced itself from meeting the daily needs of many chronically ill patients. As a result, untrained family members must pick up where healthcare leaves off, which can be a daunting prospect.
Evidence of these changes abound. Studies conducted by MetLife and repeated at various intervals show that the number of women providing basic care has grown from 9 percent in 1994 to 28 percent in 2008.3
A Disproportionate Burden on Women
The number of men providing care has increased as well but remains far below that of women. In fact, the distribution of caregiving responsibilities among the sexes is far from equitable. Not only do women shoulder two-thirds of the responsibilities but they are also often required to provide the most demanding and stressful elements of care—addressing what are known as activities of daily life (ADLs), which include eating, dressing, bathing, and using the toilet.
Irrespective of gender, caregiving is a major responsibility that requires a sustained commitment. While Darrell may be an outlier— as someone whose role as a caregiver has consumed much of his life— the majority of caregivers report extended periods of care, many taking on the role for a minimum of three years.
The Unseen Toll on Caregiver Health and Well-Being
Researchers have known for years that there can be a high toll associated with caregiving—emotionally, physically, and economically. At the extreme, evidence suggests that it can even have an impact on mortality. The degree to which the health and well-being of caregivers is negatively affected appears to be tied to their perceived level of burden and their ability, based on their underlying physical and mental health, to manage the stress.
A survey conducted by the National Alliance for Caregiving found that 53 percent of caregivers rated the emotional stress of caregiving as moderate or high. Women were significantly more likely to experience high levels of stress, as were people in fair to poor health. Caregivers providing for Alzheimer’s patients were also more at risk.
The Costs of Caregiving
Caregiving takes a toll not only on our physical health and well-being but also on our wallets, as revealed in a 2011 report titled The MetLife Study of Caregiving Costs to Working Caregivers.3 The report focused on the 10 million adult children (ages 50 and older) who serve as caregivers for their parents. Among the numerous, eye-popping statistics were these estimates of the financial toll of caregiving:
Women, once again, bear a disproportionate burden associated with caregiving—in this case, financial.
Inoculating Yourself against the Potential Pitfalls of Caregiving
There are inescapable realities to caregiving. Yet a caregiver’s ability to shift the focus, from one of burden to a beneficence and grace shared with the care recipient, has much to do with preparation, attitude, and adoption of some very specific behaviors.
Here is a short prescription for improving the journey through caregiving:
As a caregiver, it is essential that you have a simple plan for taking care of yourself—and that you stick to it. It should address exercise, good nutrition, maintaining important social relationships, honoring one’s family, and ensuring that your health needs are addressed.
Caregiving sweeps you up in a powerful current and can carry you in directions you never anticipated. It can be a turbulent and distressing journey or a transformational one—and likely both. Ultimately, when you find yourself on the other side of the experience, there is no doubt you will be forever changed and enlightened.
John Leifer has spent more than 30 years immersed in the healthcare industry as a senior healthcare executive, consultant, academician, and writer. An outspoken advocate for patients’ rights, he has published widely on the need for patients to receive appropriate, safe, effective care, including two, recent books: The Myths of Modern Medicine: The Alarming Truth about American Health Care and After You Hear It’s Cancer: A Guide to Surviving the Difficult Journey Ahead. Leifer is the founder and chief executive officer of My Cancer Advocate, a not-for-profit organization committed to empowering patients with the right information and resources needed to participate actively in their cancer care. For more information visit afteryouhearitscancer.com or e-mail mailto:firstname.lastname@example.org.
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